VEMO - 99 OOD

FDA inspections

FDA lists 1 food or dietary supplement inspection at a facility matching VEMO - 99 OOD, in 2018, as of Oct 22, 2026. It found conditions the firm was left to correct.

• Voluntary action indicated · Objectionable conditions found; FDA left corrections to the firm

  Inspected May 11, 2018

  Sofia, Bulgaria

  Listed by FDA as Vemo 99 Ltd., Limited

  7 citations posted:

  • Master manufacturing record - each batch (21 CFR 111.205(a))
  • Master manufacturing record theoretical and expected yield (21 CFR 111.210(f))
  • Packaging description, representative label (21 CFR 111.210(g))
  • Batch record - follow master (21 CFR 111.255(c))

  See all 7 citations

  • Master manufacturing record - each batch (21 CFR 111.205(a))

    You did not prepare a written master manufacturing record for each batch size of a dietary supplement that you manufactured.

  • Master manufacturing record theoretical and expected yield (21 CFR 111.210(f))

    Your master manufacturing record did not include a statement of the theoretical yield for each point, step, or stage of the manufacturing process to ensure quality control, the expected yield of the finished dietary supplement and the maximum and minimum percentages of theoretical yield beyond which a deviation investigation of a batch is necessary and material review is conducted and disposition decision is made.

  • Packaging description, representative label (21 CFR 111.210(g))

    Your master manufacturing record did not include a representative label, or a cross-reference to the physical location of the actual or representative label.

  • Batch record - follow master (21 CFR 111.255(c))

    Your batch production record did not accurately follow the appropriate master manufacturing record.

  • Batch record - component; unique identifier (21 CFR 111.260(d))

    Your batch production records did not include the unique identifier that you assigned to a component.

  • Batch record - component; identity, weight (21 CFR 111.260(e))

    Your batch production records did not include the weight or measure of each component used.

  • Batch record - packaging, labeling (21 CFR 111.260(k))

    Your batch production records did not include documentation, at the time of performance, of labeling operations.

  FEI 3006942906

We match FDA inspections to companies by facility ZIP code (or city outside the US) and company name, so an inspection filed under a different name won’t appear here. FDA publishes final classifications only, and holds some back while enforcement is pending. Posted citations may differ from FDA’s final findings. FDA Data Dashboard · How we check