Consumer Product Partners, LLC

Form 483 issued February 5, 2026 · Saint Louis, Missouri

Inspection
Jan 27 – Feb 5, 2026
Observations
4
Pages
8
FEI number
1941150

In short: On February 5, 2026, FDA issued a Form 483 with 4 observations to Consumer Product Partners, LLC in Saint Louis, Missouri (FEI 1941150) after an inspection that ran Jan 27 – Feb 5, 2026. The investigators were Chad W. Rice and Eric D. Bowles. Most observations concern quality system and materials.

At a glance

Quality system and materials account for 3 of 4 observations.

Quality system2
Materials1
Production1

What FDA observed

Preview: the opening words of each observation
  1. 01

    There was a failure to handle and store components at all times in a…

  2. 02

    The responsibilities and procedures applicable to the quality control unit…

  3. 03

    Procedures designed to prevent objectionable microorganisms in drug products not required to be…

  4. 04

    Procedures describing the handling of all written and oral complaints regarding a drug…

The full 483

Plus the full detail behind each one, exactly as FDA wrote it.

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This inspection in context

Questions about this 483

What did FDA find at Consumer Product Partners, LLC?

FDA listed 4 observations on this Form 483, mostly about quality system, materials and production. The opening words of each observation are shown on this page.

Who inspected Consumer Product Partners, LLC?

Chad W. Rice and Eric D. Bowles are named on this Form 483, for the inspection of Jan 27 – Feb 5, 2026. Each investigator has a profile showing what they cite most.

When was Consumer Product Partners, LLC inspected by FDA?

The inspection ran Jan 27 – Feb 5, 2026, and the Form 483 is dated February 5, 2026.

How do I get the full Form 483 for Consumer Product Partners, LLC?

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