Consumer Product Partners, LLC

FDA inspection history across 2 sites, 2021 to 2026

3
Form 483s
1
Warning letter

Every document, by year

  • Form 483
  • Warning letter

2021: one Form 483; 2022: one warning letter; 2023: one Form 483; 2026: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2021–23Two Form 483s and one warning letter, at St. Louis, Missouri.
  2. 2021The longest 483 on file: 6 observations over 6 pages at St. Louis, Missouri.
  3. 2026One Form 483, at Saint Louis, Missouri.

Cited most

Across all Consumer Product Partners observations on file

The complete Consumer Product Partners file.

All 4 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$396

The price of the documents, added to your cart together

Sites

Documents

4 on file, newest first
DateDocumentPrice
2026-02-05483 Form 483$99
2023-06-14483 Form 483$99
2022-03-31Warning letter Warning letter$99
2021-10-13483 Form 483$99

FEI number 1941150 · most recent document Feb 5, 2026

About Consumer Product Partners, LLC

How many FDA Form 483s has Consumer Product Partners, LLC received?

FDA Intel has 3 Form 483s on file for Consumer Product Partners, LLC; the most recent is dated Feb 5, 2026.

When was Consumer Product Partners, LLC last inspected by FDA?

The most recent FDA inspection document on file for Consumer Product Partners, LLC is a Form 483 dated Feb 5, 2026, for the site in Saint Louis, Missouri.

What did FDA cite at Consumer Product Partners, LLC?

The regulations cited most in the observations on file for Consumer Product Partners, LLC are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.22 (Responsibilities of quality control unit), 3 times; 21 CFR 211.192 (Production record review), 2 times.

Has Consumer Product Partners, LLC received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Consumer Product Partners, LLC; the most recent is dated Mar 31, 2022.