Intervet International GMBH
FDA inspection history in Unterscheissheim, 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 Unterscheissheim, Germany.
Cited most
Across all Intervet International observations on file
- 21 CFR 211.122Materials examination and usage criteria1
- 21 CFR 211.165(e)Testing and release for distribution1
The complete Intervet International file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Unterscheissheim, Germany
One Form 483 · 2023 · 2 observations
Latest: Form 483, Apr 28, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-04-28 | 483 Form 483 | Unterscheissheim, Germany | 2 | $99 |
Investigators on these documents
FEI number 3003517550 · most recent document Apr 28, 2023
About Intervet International GMBH
How many FDA Form 483s has Intervet International GMBH received?
FDA Intel has 1 Form 483 on file for Intervet International GMBH; the most recent is dated Apr 28, 2023.
When was Intervet International GMBH last inspected by FDA?
The most recent FDA inspection document on file for Intervet International GMBH is a Form 483 dated Apr 28, 2023, for the site in Unterscheissheim, Germany.
What did FDA cite at Intervet International GMBH?
The regulations cited most in the observations on file for Intervet International GMBH are 21 CFR 211.122 (Materials examination and usage criteria), 1 time; 21 CFR 211.165(e) (Testing and release for distribution), 1 time.