Eckert & Ziegler Radiopharma GmbH
FDA inspection history in Berlin, Germany, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Berlin, Germany.
Cited most
Across all Eckert & Ziegler Radiopharma observations on file
- 21 CFR 211.42Design and construction features6
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
The complete Eckert & Ziegler Radiopharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Berlin, Germany
One Form 483 · 2019 · 13 observations
Latest: Form 483, Aug 23, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-08-23 | 483 Form 483 | Berlin, Germany | 13 | $99 |
Investigators on these documents
FEI number 3005746948 · most recent document Aug 23, 2019
About Eckert & Ziegler Radiopharma GmbH
How many FDA Form 483s has Eckert & Ziegler Radiopharma GmbH received?
FDA Intel has 1 Form 483 on file for Eckert & Ziegler Radiopharma GmbH; the most recent is dated Aug 23, 2019.
When was Eckert & Ziegler Radiopharma GmbH last inspected by FDA?
The most recent FDA inspection document on file for Eckert & Ziegler Radiopharma GmbH is a Form 483 dated Aug 23, 2019, for the site in Berlin, Germany.
What did FDA cite at Eckert & Ziegler Radiopharma GmbH?
The regulations cited most in the observations on file for Eckert & Ziegler Radiopharma GmbH are 21 CFR 211.42 (Design and construction features), 6 times; 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time.