FDA Inspection
FUJIFILM Healthcare Americas CorporationFUJIFILM Healthcare Americas Corporation – FDA Inspection, Oct 31, 2016
Record Details
This FDA Inspection record concerns FUJIFILM Healthcare Americas Corporation, with an inspection on October 31, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 945c2309-d1e2-4202-b58d-2bbd97355afa
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 991423
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of FUJIFILM Healthcare Americas Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 21, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 29, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| November 10, 2016 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 19, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 12, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for FUJIFILM Healthcare Americas Corporation
- FDA Inspection 1095860 - 2019-06-21
- FDA Inspection 1046796 - 2018-03-29
- FDA Inspection 994698 - 2016-11-10
- FDA Inspection 919044 - 2015-02-19
- FDA Inspection 810738 - 2012-12-12
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