FDA Inspection 950162 — Shionogi Pharma Co. Ltd.
The FDA completed an inspection of Shionogi Pharma Co. Ltd. on Dec 4, 2015 in Tokushima. 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
- Dec 4, 2015
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Tokushima (Japan)