FDA Inspection 974319 — Miyoshi America, Inc
The FDA completed an inspection of Miyoshi America, Inc on Jun 3, 2016 in Dayville, CT. 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
- Jun 3, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Dayville, CT (United States)