Takeda Manufacturing Singapore Pte. Ltd.
FDA inspection history in Singapore, Singapore, 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 Singapore, Singapore.
Cited most
Across all Takeda Manufacturing Singapore Pte. observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.25Personnel qualifications1
The complete Takeda Manufacturing Singapore Pte. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Singapore, Singapore
One Form 483 · 2022 · 2 observations
Latest: Form 483, Nov 18, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-18 | 483 Form 483 | Singapore, Singapore | 2 | $99 |
Investigators on these documents
FEI number 3009153654 · most recent document Nov 18, 2022
About Takeda Manufacturing Singapore Pte. Ltd.
How many FDA Form 483s has Takeda Manufacturing Singapore Pte. Ltd. received?
FDA Intel has 1 Form 483 on file for Takeda Manufacturing Singapore Pte. Ltd.; the most recent is dated Nov 18, 2022.
When was Takeda Manufacturing Singapore Pte. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Takeda Manufacturing Singapore Pte. Ltd. is a Form 483 dated Nov 18, 2022, for the site in Singapore, Singapore.
What did FDA cite at Takeda Manufacturing Singapore Pte. Ltd.?
The regulations cited most in the observations on file for Takeda Manufacturing Singapore Pte. Ltd. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.25 (Personnel qualifications), 1 time.