FDA Inspection 890110 — Hoya Corporation - Pentax Life Division
The FDA completed an inspection of Hoya Corporation - Pentax Life Division on Jul 15, 2014 in Akishima. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 15, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Akishima (Japan)