Zoetis Belgium S.A.
FDA inspection history in Ottignies-Louvain-la-Neuve, Belgium, 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 Ottignies-Louvain-la-Neuve, Belgium.
Cited most
Across all Zoetis Belgium observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.113(b)Control of microbiological contamination1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Zoetis Belgium file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ottignies-Louvain-la-Neuve, Belgium
One Form 483 · 2022 · 5 observations
Latest: Form 483, Nov 22, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-22 | 483 Form 483 | Ottignies-Louvain-la-Neuve, Belgium | 5 | $99 |
Investigators on these documents
FEI number 3010087842 · most recent document Nov 22, 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 Nov 22, 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 Nov 22, 2022, for the site in Ottignies-Louvain-la-Neuve, Belgium.
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 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.113(b) (Control of microbiological contamination), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time.