FDA Inspection 1113539 — Tomita Pharmaceutical Co., Ltd.

Tomita Pharmaceutical Co., Ltd. — FEI 3002808375

The FDA completed an inspection of Tomita Pharmaceutical Co., Ltd. on Nov 8, 2019 in Naruto. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 8, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Naruto (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.