FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022
FDA inspection history on file, 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.
Cited most
Across all FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022 observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022 file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-18 | 483 Form 483 | — | 2 | $99 |
Investigators on these documents
FEI number 300915365 · most recent document Nov 18, 2022
About FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022
How many FDA Form 483s has FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022 received?
FDA Intel has 1 Form 483 on file for FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022; the most recent is dated Nov 18, 2022.
When was FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022 last inspected by FDA?
The most recent FDA inspection document on file for FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022 is a Form 483 dated Nov 18, 2022.
What did FDA cite at FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022?
The regulations cited most in the observations on file for FDA Form 483 Takeda Manufacturing, Singapore, Nov 2022 are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.