Morishita Jintan Co. Ltd.
FDA inspection history in Tagacho, Japan, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Tagacho, Japan.
Cited most
Across all Morishita Jintan Co. observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.166(c)(2)Stability testing1
The complete Morishita Jintan Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tagacho, Japan
One Form 483 · 2023 · 3 observations
Latest: Form 483, May 19, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-05-19 | 483 Form 483 | Tagacho, Japan | 3 | $99 |
Investigators on these documents
FEI number 3007328931 · most recent document May 19, 2023
About Morishita Jintan Co. Ltd.
How many FDA Form 483s has Morishita Jintan Co. Ltd. received?
FDA Intel has 1 Form 483 on file for Morishita Jintan Co. Ltd.; the most recent is dated May 19, 2023.
When was Morishita Jintan Co. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Morishita Jintan Co. Ltd. is a Form 483 dated May 19, 2023, for the site in Tagacho, Japan.
What did FDA cite at Morishita Jintan Co. Ltd.?
The regulations cited most in the observations on file for Morishita Jintan Co. Ltd. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.166(c)(2) (Stability testing), 1 time.