Haupt Pharma Muenster GmbH
FDA inspection history in Muenster, Germany, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Muenster, Germany.
Cited most
Across all Haupt Pharma Muenster observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Haupt Pharma Muenster file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Muenster, Germany
One Form 483 · 2018 · 3 observations
Latest: Form 483, Jul 6, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-07-06 | 483 Form 483 | Muenster, Germany | 3 | $99 |
Investigators on these documents
FEI number 3006010798 · most recent document Jul 6, 2018
About Haupt Pharma Muenster GmbH
How many FDA Form 483s has Haupt Pharma Muenster GmbH received?
FDA Intel has 1 Form 483 on file for Haupt Pharma Muenster GmbH; the most recent is dated Jul 6, 2018.
When was Haupt Pharma Muenster GmbH last inspected by FDA?
The most recent FDA inspection document on file for Haupt Pharma Muenster GmbH is a Form 483 dated Jul 6, 2018, for the site in Muenster, Germany.
What did FDA cite at Haupt Pharma Muenster GmbH?
The regulations cited most in the observations on file for Haupt Pharma Muenster GmbH are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.68(b) (Automatic, mechanical, and electronic equipment), 1 time.