PediFix, Inc.
FDA inspection history in Brewster, New York, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Brewster, New York.
Cited most
Across all PediFix observations on file
- 21 CFR 211.22(a)Responsibilities of quality control unit1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete PediFix file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Brewster, New York
One Form 483 · 2024 · 2 observations
Latest: Form 483, Feb 12, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-02-12 | 483 Form 483 | Brewster, New York | 2 | $99 |
Investigators on these documents
FEI number 3009710062 · most recent document Feb 12, 2024
About PediFix, Inc.
How many FDA Form 483s has PediFix, Inc. received?
FDA Intel has 1 Form 483 on file for PediFix, Inc.; the most recent is dated Feb 12, 2024.
When was PediFix, Inc. last inspected by FDA?
The most recent FDA inspection document on file for PediFix, Inc. is a Form 483 dated Feb 12, 2024, for the site in Brewster, New York.
What did FDA cite at PediFix, Inc.?
The regulations cited most in the observations on file for PediFix, Inc. are 21 CFR 211.22(a) (Responsibilities of quality control unit), 1 time; 21 CFR 211.68(b) (Automatic, mechanical, and electronic equipment), 1 time.