FDA Inspection 705556 — HOYA Corporation PENTAX Miyagi Factory
The FDA completed an inspection of HOYA Corporation PENTAX Miyagi Factory on Dec 16, 2010 in Kurihara. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 16, 2010
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kurihara (Japan)