Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun
FDA inspection history in Gifa, 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 Gifa, Japan.
Cited most
Across all Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun observations on file
- 21 CFR 211.125Labeling issuance1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Gifa, Japan
One Form 483 · 2022 · 3 observations
Latest: Form 483, Sep 2, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-02 | 483 Form 483 | Gifa, Japan | 3 | $99 |
Investigators on these documents
FEI number 3008927877 · most recent document Sep 2, 2022
About Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun
How many FDA Form 483s has Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun received?
FDA Intel has 1 Form 483 on file for Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun; the most recent is dated Sep 2, 2022.
When was Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun last inspected by FDA?
The most recent FDA inspection document on file for Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun is a Form 483 dated Sep 2, 2022, for the site in Gifa, Japan.
What did FDA cite at Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun?
The regulations cited most in the observations on file for Meiji Seika Pharma Co., Ltd. 2890 Kitagata, Kitagata-Cho, Motosa-Gun are 21 CFR 211.125 (Labeling issuance), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.