Nippon Kayaku Pharmatech Co., Ltd. FDA Record
Nippon Kayaku Pharmatech Co., Ltd. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Nippon Kayaku Pharmatech Co., Ltd." is on file.
- Latest inspection
- Nov 25, 2022 · VAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 1 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Nov 25, 2022 | Toyama, Japan | Drugs | Voluntary Action Indicated (VAI) | 3008538640 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3008538640 | Toyama, Japan | 1 | Nov 25, 2022 |
Nippon Kayaku Pharmatech Co., Ltd. and the FDA: common questions
Has Nippon Kayaku Pharmatech Co., Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Nippon Kayaku Pharmatech Co., Ltd." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Nippon Kayaku Pharmatech Co., Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Nippon Kayaku Pharmatech Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Nippon Kayaku Pharmatech Co., Ltd.?
The most recent FDA inspection on file ended Nov 25, 2022 at Toyama, Japan and was classified VAI. FDA has 1 inspection of Nippon Kayaku Pharmatech Co., Ltd. on file.
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