Meiji Seika Pharmatech Co., Ltd.
FDA inspection history in Odawara, 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 Odawara, Japan.
Cited most
Across all Meiji Seika Pharmatech Co. observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Meiji Seika Pharmatech Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Odawara, Japan
One Form 483 · 2022 · 3 observations
Latest: Form 483, Apr 8, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-04-08 | 483 Form 483 | Odawara, Japan | 3 | $99 |
Investigators on these documents
FEI number 3015407855 · most recent document Apr 8, 2022
About Meiji Seika Pharmatech Co., Ltd.
How many FDA Form 483s has Meiji Seika Pharmatech Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Meiji Seika Pharmatech Co., Ltd.; the most recent is dated Apr 8, 2022.
When was Meiji Seika Pharmatech Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Meiji Seika Pharmatech Co., Ltd. is a Form 483 dated Apr 8, 2022, for the site in Odawara, Japan.
What did FDA cite at Meiji Seika Pharmatech Co., Ltd.?
The regulations cited most in the observations on file for Meiji Seika Pharmatech Co., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.