FDA Inspection
FujiFilm Healthcare Americas CorporationFujiFilm Healthcare Americas Corporation – FDA Inspection, Aug 4, 2009
Record Details
This FDA Inspection record concerns FujiFilm Healthcare Americas Corporation, with an inspection on August 4, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 4, 2009
- Product Type
- Devices
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ID · e7c6aa0b-6b40-4da6-b692-cd4c13193fa7
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 605222
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
Other FDA inspections of FujiFilm Healthcare Americas Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2017 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 8, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 1, 2010 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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