Vet Pharma Friesoythe GmbH
FDA inspection history in Friesoythe, Germany, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Friesoythe, Germany.
Cited most
Across all Vet Pharma Friesoythe observations on file
- 21 CFR 211.42(c)(10)(iv)Design and construction features2
- 21 CFR 111.255(b)What is the requirement to establish a batch production record?1
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.113(b)Control of microbiological contamination1
- 21 CFR 211.192Production record review1
The complete Vet Pharma Friesoythe file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Friesoythe, Germany
One Form 483 · 2023 · 9 observations
Latest: Form 483, Mar 24, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-03-24 | 483 Form 483 | Friesoythe, Germany | 9 | $99 |
Investigators on these documents
FEI number 3002808866 · most recent document Mar 24, 2023
About Vet Pharma Friesoythe GmbH
How many FDA Form 483s has Vet Pharma Friesoythe GmbH received?
FDA Intel has 1 Form 483 on file for Vet Pharma Friesoythe GmbH; the most recent is dated Mar 24, 2023.
When was Vet Pharma Friesoythe GmbH last inspected by FDA?
The most recent FDA inspection document on file for Vet Pharma Friesoythe GmbH is a Form 483 dated Mar 24, 2023, for the site in Friesoythe, Germany.
What did FDA cite at Vet Pharma Friesoythe GmbH?
The regulations cited most in the observations on file for Vet Pharma Friesoythe GmbH are 21 CFR 211.42(c)(10)(iv) (Design and construction features), 2 times; 21 CFR 111.255(b) (What is the requirement to establish a batch production record?), 1 time; 21 CFR 211.100(a) (Written procedures; deviations), 1 time.