FDA Inspection
HOYA Corporation PENTAX Miyagi FactoryHOYA Corporation PENTAX Miyagi Factory – FDA Inspection, Dec 16, 2010
Record Details
This FDA Inspection record concerns HOYA Corporation PENTAX Miyagi Factory, with an inspection on December 16, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 16, 2010
- Product Type
- Devices
View Company Profile
ID · a64af382-d217-45a2-bce9-96829fe79523
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 705556
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of HOYA Corporation PENTAX Miyagi Factory
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 3, 2023 | Not classified | Office of Inspections and Investigations | |
| September 4, 2018 | Not classified | Office of Inspections and Investigations | |
| April 24, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 21, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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