Pfizer Manufacturing Deutschland GmbH
FDA inspection history in Freiburg im Breisgau, Germany, 2019 to 2020
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019–20Two Form 483s, at Freiburg im Breisgau, Germany.
- 2019The longest 483 on file: 3 observations over 3 pages at Freiburg im Breisgau, Germany.
Cited most
Across all Pfizer Manufacturing Deutschland observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Pfizer Manufacturing Deutschland file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Freiburg im Breisgau, Germany
Two Form 483s · 2019 to 2020 · 6 observations
Latest: Form 483, Feb 7, 2020 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-02-07 | 483 Form 483 | Freiburg im Breisgau, Germany | 3 | $99 |
| 2019-03-08 | 483 Form 483 | Freiburg im Breisgau, Germany | 3 | $99 |
Investigators on these documents
FEI number 3002807097 · most recent document Feb 7, 2020
About Pfizer Manufacturing Deutschland GmbH
How many FDA Form 483s has Pfizer Manufacturing Deutschland GmbH received?
FDA Intel has 2 Form 483s on file for Pfizer Manufacturing Deutschland GmbH; the most recent is dated Feb 7, 2020.
When was Pfizer Manufacturing Deutschland GmbH last inspected by FDA?
The most recent FDA inspection document on file for Pfizer Manufacturing Deutschland GmbH is a Form 483 dated Feb 7, 2020, for the site in Freiburg im Breisgau, Germany.
What did FDA cite at Pfizer Manufacturing Deutschland GmbH?
The regulations cited most in the observations on file for Pfizer Manufacturing Deutschland GmbH are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.198 (Complaint files), 1 time.