Zoetis Belgium S.A
FDA inspection history in RATHDRUM, Ireland, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at RATHDRUM, Ireland.
Cited most
Across all Zoetis Belgium observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Zoetis Belgium file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
RATHDRUM, Ireland
One Form 483 · 2022 · 4 observations
Latest: Form 483, Mar 25, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-03-25 | 483 Form 483 | RATHDRUM, Ireland | 4 | $99 |
Investigators on these documents
FEI number 3015422006 · most recent document Mar 25, 2022
About Zoetis Belgium S.A
How many FDA Form 483s has Zoetis Belgium S.A received?
FDA Intel has 1 Form 483 on file for Zoetis Belgium S.A; the most recent is dated Mar 25, 2022.
When was Zoetis Belgium S.A last inspected by FDA?
The most recent FDA inspection document on file for Zoetis Belgium S.A is a Form 483 dated Mar 25, 2022, for the site in RATHDRUM, Ireland.
What did FDA cite at Zoetis Belgium S.A?
The regulations cited most in the observations on file for Zoetis Belgium S.A are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.186 (Master production and control records), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.