Hisamitsu Pharmaceutical Co., Inc.
FDA inspection history in Tosu, Japan, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Tosu, Japan.
Cited most
Across all Hisamitsu Pharmaceutical Co. observations on file
- 21 CFR 211.165Testing and release for distribution2
- 21 CFR 211.192Production record review2
- 21 CFR 211.160General requirements1
- 21 CFR 211.194Laboratory records1
The complete Hisamitsu Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tosu, Japan
One Form 483 · 2019 · 4 observations
Latest: Form 483, May 31, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-31 | 483 Form 483 | Tosu, Japan | 4 | $99 |
Investigators on these documents
FEI number 1000266995 · most recent document May 31, 2019
About Hisamitsu Pharmaceutical Co., Inc.
How many FDA Form 483s has Hisamitsu Pharmaceutical Co., Inc. received?
FDA Intel has 1 Form 483 on file for Hisamitsu Pharmaceutical Co., Inc.; the most recent is dated May 31, 2019.
When was Hisamitsu Pharmaceutical Co., Inc. last inspected by FDA?
The most recent FDA inspection document on file for Hisamitsu Pharmaceutical Co., Inc. is a Form 483 dated May 31, 2019, for the site in Tosu, Japan.
What did FDA cite at Hisamitsu Pharmaceutical Co., Inc.?
The regulations cited most in the observations on file for Hisamitsu Pharmaceutical Co., Inc. are 21 CFR 211.165 (Testing and release for distribution), 2 times; 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.160 (General requirements), 1 time.