KVP Pharma Veterinär Produkte GmbH
FDA inspection history in Kiel, 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 Kiel, Germany.
Cited most
Across all KVP Pharma Veterinär Produkte observations on file
- 21 CFR 211.160(b)General requirements1
The complete KVP Pharma Veterinär Produkte file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Kiel, Germany
One Form 483 · 2023 · 1 observation
Latest: Form 483, Mar 24, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-03-24 | 483 Form 483 | Kiel, Germany | 1 | $99 |
FEI number 3004159824 · most recent document Mar 24, 2023
About KVP Pharma Veterinär Produkte GmbH
How many FDA Form 483s has KVP Pharma Veterinär Produkte GmbH received?
FDA Intel has 1 Form 483 on file for KVP Pharma Veterinär Produkte GmbH; the most recent is dated Mar 24, 2023.
When was KVP Pharma Veterinär Produkte GmbH last inspected by FDA?
The most recent FDA inspection document on file for KVP Pharma Veterinär Produkte GmbH is a Form 483 dated Mar 24, 2023, for the site in Kiel, Germany.
What did FDA cite at KVP Pharma Veterinär Produkte GmbH?
The regulations cited most in the observations on file for KVP Pharma Veterinär Produkte GmbH are 21 CFR 211.160(b) (General requirements), 1 time.