Ishihara Sangyo Kaisha, Ltd.
FDA inspection history in Yokkaichi, Japan, 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 Yokkaichi, Japan.
Cited most
Across all Ishihara Sangyo Kaisha observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.192Production record review1
The complete Ishihara Sangyo Kaisha file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Yokkaichi, Japan
One Form 483 · 2022 · 2 observations
Latest: Form 483, Sep 9, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-09 | 483 Form 483 | Yokkaichi, Japan | 2 | $99 |
Investigators on these documents
FEI number 3002807309 · most recent document Sep 9, 2022
About Ishihara Sangyo Kaisha, Ltd.
How many FDA Form 483s has Ishihara Sangyo Kaisha, Ltd. received?
FDA Intel has 1 Form 483 on file for Ishihara Sangyo Kaisha, Ltd.; the most recent is dated Sep 9, 2022.
When was Ishihara Sangyo Kaisha, Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Ishihara Sangyo Kaisha, Ltd. is a Form 483 dated Sep 9, 2022, for the site in Yokkaichi, Japan.
What did FDA cite at Ishihara Sangyo Kaisha, Ltd.?
The regulations cited most in the observations on file for Ishihara Sangyo Kaisha, Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time.