FDA Inspection
HOYA Corporation PENTAX Miyagi FactoryHOYA Corporation PENTAX Miyagi Factory – FDA Inspection, Sep 4, 2018
Record Details
This FDA Inspection record concerns HOYA Corporation PENTAX Miyagi Factory, with an inspection on September 4, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- September 4, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · f2ee4415-d095-48d2-965b-c5052e4a1c52
Inspection Facts
- Inspection number
- 1124077
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
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 | |
| April 24, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 21, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 16, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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