Dabur India Ltd

FDA inspections

FDA lists 1 food or dietary supplement inspection at a facility matching Dabur India Ltd, in 2016, 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 Jul 15, 2016

  Ghaziabad, India

  Listed by FDA as Dabur India Limited, Sahibabad Unit

  4 citations posted:

  • Equipment - design - suitable (21 CFR 111.27(a))
  • Exempted, periodic testing; quality control (21 CFR 111.75(d)(2))
  • Master manufacturing record - specific actions; quality (21 CFR 111.210(h)(3))
  • Batch record - results; testing, examination; batch (21 CFR 111.260(h))

  Full citation text

  • Equipment - design - suitable (21 CFR 111.27(a))

    You did not use equipment or utensils of appropriate design, construction, and workmanship to enable them to be adequately cleaned and properly maintained.

  • Exempted, periodic testing; quality control (21 CFR 111.75(d)(2))

    Your quality control personnel did not review and approve the documentation of why an exempted product specification is met without verification through periodic testing of the finished batch.

  • Master manufacturing record - specific actions; quality (21 CFR 111.210(h)(3))

    The written instructions in your master manufacturing record did not include specific actions necessary to perform and verify points, steps, or stages in the manufacturing process where control is necessary to ensure the quality of the dietary supplement.

  • Batch record - results; testing, examination; batch (21 CFR 111.260(h))

    Your batch production records did not include the results of testing or examination performed during batch production, or a cross-reference to such results.

  FEI 3004326829

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