P & L Developments, LLC: due-diligence report
Public-record summary and buyer worksheet. Records can be incomplete; a listing is not product approval, an audit result or a guarantee of suitability. This report updates as source records change. Print a dated copy to retain the version you reviewed.
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Profile last verified: Nov 1, 2026. Report printed / reviewed on: ____________________
Certifications and licences
NSF/ANSI 455-2 GMP for Dietary Supplements
Issuer: NSF. Registry status: active. Checked: Nov 1, 2026.
Reference: Not recorded. Expiry: Not recorded.
Scope: Not recorded here; confirm with the registry and manufacturer.
Registry source: https://info.nsf.org/Certified/455GMP/Listings.asp?NSF/ANSI 455-4 GMP for OTC Drugs
Issuer: NSF. Registry status: active. Checked: Nov 1, 2026.
Reference: Not recorded. Expiry: Not recorded.
Scope: Not recorded here; confirm with the registry and manufacturer.
Registry source: https://info.nsf.org/Certified/455GMP/Listings.asp?Facilities
P & L Developments, LLC, 200 Hicks Street, Westbury, NY, 11590, US — packaging; source: NSF/ANSI 455-2; checked Nov 1, 2026.
P & L Developments, LLC, 11865 South Alameda Street, Lynwood, CA, 90262, US — manufacturing; source: NSF/ANSI 455-2; checked Nov 1, 2026.
P & L Developments, LLC, 513 Old Griffin Road, Piedmont, SC, 28673, US — manufacturing; source: NSF/ANSI 455-2; checked Nov 1, 2026.
P & L Developments, LLC, 11840 South Alameda Street, Lynwood, CA, 90262, US — packaging; source: NSF/ANSI 455-2; checked Nov 1, 2026.
FDA inspection history
Dataset date: Oct 22, 2026. Facility records are matched by company and location; confirm that the site is the one in your quote. FDA inspection source.
Apr 3, 2012 — NAI: No action indicated
P&L Developments, LLC, Lynwood, California, United States. FEI: 1000160562; inspection: 776724.
Food Composition, Standards, Labeling and Econ, Foodborne Biological Hazards
21 CFR 211.142: Written warehousing procedures established/followed
21 CFR 211.160(a): Following/documenting laboratory controls
21 CFR 211.166(a)(3): Valid stability test methods
21 CFR 211.180(e)(2): Items to cover on annual reviews
21 CFR 211.194(a)(2): Laboratory Test Method Verification
21 CFR 211.194(a)(4): Data secured in course of each test
FDA recalls
Dataset date: Oct 27, 2026. Recall matches use company names and may concern a different product or facility.
No matched recall events in the imported dataset. This is not proof of a recall-free history.
Company website claims — not registry verified
Last website check: Oct 16, 2026.
“PLD offers a full range of private label liquid and solid dose OTC pharmaceutical and consumer health care products, including first aid and beauty care items.”
Last seen Oct 16, 2026. http://www.pldevelopments.com/products-home/
“Our capabilities include bottling, blistering, cartoning, pouching, clamshell, twinpacks, vial packs, and many other types of creative packaging options for both liquid and solid dosage forms.”
Last seen Oct 16, 2026. http://www.pldevelopments.com/capabilities/packaging/
Evidence to request from the manufacturer
Public records cannot answer these questions. Mark each item after reviewing the evidence. Blank means not assessed, not a failed audit. Notes entered here are not saved or included in a shared URL.
Request role-specific training records and the named quality contact.
21 CFR 111.12Request a site walkthrough, sanitation controls and equipment maintenance records (also §111.25).
21 CFR 111.20Request written identity, purity, strength, composition and contaminant specifications for your product.
21 CFR 111.70Ask how each dietary ingredient is identified and how suppliers and certificates of analysis are qualified.
21 CFR 111.75Request quality control procedures, release authority and handling of deviations and rejected batches.
21 CFR 111.105Request the approved product-specific master manufacturing record and change-control process.
21 CFR 111.205Review a completed batch record with traceability to components, processing and release.
21 CFR 111.255Request scientifically valid test methods, sampling plans and laboratory controls for your specifications.
21 CFR 111.315Request procedures that prevent label mix-ups and control packaging and label reconciliation.
21 CFR 111.403Ask how storage conditions protect identity, purity, strength and composition during holding and distribution.
21 CFR 111.453Request complaint review and investigation procedures; discuss returned-product controls under §111.503.
21 CFR 111.553Confirm retention and access to records supporting your batches.
21 CFR 111.605