Mitsubishi Tanabe Pharma Factory Ltd.
FDA inspection history in Onoda, Japan, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Onoda, Japan.
Cited most
Across all Mitsubishi Tanabe Pharma Factory observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.67Equipment cleaning and maintenance1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
- 21 CFR 211.80General requirements1
The complete Mitsubishi Tanabe Pharma Factory file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Onoda, Japan
One Form 483 · 2024
Latest: Form 483, Jan 19, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-01-19 | 483 Form 483 | Onoda, Japan | — | $99 |
Investigators on these documents
FEI number 3002808316 · most recent document Jan 19, 2024
About Mitsubishi Tanabe Pharma Factory Ltd.
How many FDA Form 483s has Mitsubishi Tanabe Pharma Factory Ltd. received?
FDA Intel has 1 Form 483 on file for Mitsubishi Tanabe Pharma Factory Ltd.; the most recent is dated Jan 19, 2024.
When was Mitsubishi Tanabe Pharma Factory Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Mitsubishi Tanabe Pharma Factory Ltd. is a Form 483 dated Jan 19, 2024, for the site in Onoda, Japan.
What did FDA cite at Mitsubishi Tanabe Pharma Factory Ltd.?
The regulations cited most in the observations on file for Mitsubishi Tanabe Pharma Factory Ltd. are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.