Drug factory · FDA FEI 3002806334
Ajinomoto Co., Inc.
1730 Oazahinaga, Yokkaichi, Japan
Problems found, fixed voluntarily at FDA's last inspection, Nov 14, 2025.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
3 drug inspections on record since 2011: 0 with no problems, 3 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Tipiracil and Trifluridine | Makes the active ingredient and tests it | Taiho Pharmaceutical Co., Ltd. | 64842-1020, 64842-1025 |
| Viltolarsen | Makes the active ingredient | NS Pharma, Inc. | 73292-011 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Nov 14, 2025 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Feb 22, 2019 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Sep 29, 2011 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture.