Nippon Rika CO., Ltd.
FDA inspection history in ASHIKAGA, Japan, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at ASHIKAGA, Japan.
Cited most
Across all Nippon Rika CO. observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
The complete Nippon Rika CO. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
ASHIKAGA, Japan
One Form 483 · 2025 · 7 observations
Latest: Form 483, Jul 4, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-07-04 | 483 Form 483 | ASHIKAGA, Japan | 7 | $99 |
Investigators on these documents
FEI number 3002807731 · most recent document Jul 4, 2025
About Nippon Rika CO., Ltd.
How many FDA Form 483s has Nippon Rika CO., Ltd. received?
FDA Intel has 1 Form 483 on file for Nippon Rika CO., Ltd.; the most recent is dated Jul 4, 2025.
When was Nippon Rika CO., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Nippon Rika CO., Ltd. is a Form 483 dated Jul 4, 2025, for the site in ASHIKAGA, Japan.
What did FDA cite at Nippon Rika CO., Ltd.?
The regulations cited most in the observations on file for Nippon Rika CO., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.166 (Stability testing), 1 time.