Takeda Manufacturing Austria AG
FDA inspection history in WIEN, Austria, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at WIEN, Austria.
Cited most
Across all Takeda Manufacturing Austria AG observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
The complete Takeda Manufacturing Austria AG file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
WIEN, Austria
One Form 483 · 2022 · 3 observations
Latest: Form 483, Jun 24, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-06-24 | 483 Form 483 | WIEN, Austria | 3 | $99 |
Investigators on these documents
FEI number 3002807133 · most recent document Jun 24, 2022
About Takeda Manufacturing Austria AG
How many FDA Form 483s has Takeda Manufacturing Austria AG received?
FDA Intel has 1 Form 483 on file for Takeda Manufacturing Austria AG; the most recent is dated Jun 24, 2022.
When was Takeda Manufacturing Austria AG last inspected by FDA?
The most recent FDA inspection document on file for Takeda Manufacturing Austria AG is a Form 483 dated Jun 24, 2022, for the site in WIEN, Austria.
What did FDA cite at Takeda Manufacturing Austria AG?
The regulations cited most in the observations on file for Takeda Manufacturing Austria AG are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.192 (Production record review), 1 time.