FDA Inspection
FUJIFILM Healthcare Manufacturing Corp.FUJIFILM Healthcare Manufacturing Corp. – FDA Inspection, Mar 10, 2023
Record Details
This FDA Inspection record concerns FUJIFILM Healthcare Manufacturing Corp., with an inspection on March 10, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 66a06d95-9a25-4685-9249-7c660ae2dc0d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1200950
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of FUJIFILM Healthcare Manufacturing Corp.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 14, 2016 | Not classified | Office of Inspections and Investigations | |
| February 19, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for FUJIFILM Healthcare Manufacturing Corp.
- FDA Inspection 996016 - 2016-12-14
- FDA Inspection 870122 - 2014-02-19
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