Takeda Ireland Ltd.
FDA inspection history in Dublin, Ireland, 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 Dublin, Ireland.
Cited most
Across all Takeda Ireland observations on file
- 21 CFR 211.166Stability testing1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.25Personnel qualifications1
The complete Takeda Ireland file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Dublin, Ireland
One Form 483 · 2022 · 6 observations
Latest: Form 483, Feb 4, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-02-04 | 483 Form 483 | Dublin, Ireland | 6 | $99 |
FEI number 3006687027 · most recent document Feb 4, 2022
About Takeda Ireland Ltd.
How many FDA Form 483s has Takeda Ireland Ltd. received?
FDA Intel has 1 Form 483 on file for Takeda Ireland Ltd.; the most recent is dated Feb 4, 2022.
When was Takeda Ireland Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Takeda Ireland Ltd. is a Form 483 dated Feb 4, 2022, for the site in Dublin, Ireland.
What did FDA cite at Takeda Ireland Ltd.?
The regulations cited most in the observations on file for Takeda Ireland Ltd. are 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.194 (Laboratory records), 1 time.