Playtex Manufacturing Inc.
FDA inspection history in Sidney, Ohio, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Sidney, Ohio.
Cited most
Across all Playtex Manufacturing observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.67(b)Equipment cleaning and maintenance1
The complete Playtex Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Sidney, Ohio
One Form 483 · 2025 · 6 observations
Latest: Form 483, Apr 7, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-04-07 | 483 Form 483 | Sidney, Ohio | 6 | $99 |
Investigators on these documents
FEI number 3000717960 · most recent document Apr 7, 2025
About Playtex Manufacturing Inc.
How many FDA Form 483s has Playtex Manufacturing Inc. received?
FDA Intel has 1 Form 483 on file for Playtex Manufacturing Inc.; the most recent is dated Apr 7, 2025.
When was Playtex Manufacturing Inc. last inspected by FDA?
The most recent FDA inspection document on file for Playtex Manufacturing Inc. is a Form 483 dated Apr 7, 2025, for the site in Sidney, Ohio.
What did FDA cite at Playtex Manufacturing Inc.?
The regulations cited most in the observations on file for Playtex Manufacturing Inc. are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.