FDA Inspection
FUJIFILM Healthcare Manufacturing Corporation, MIE OfficeFUJIFILM Healthcare Manufacturing Corporation, MIE Office – FDA Inspection, Dec 9, 2010
Record Details
This FDA Inspection record concerns FUJIFILM Healthcare Manufacturing Corporation, MIE Office, with an inspection on December 9, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 9, 2010
- Product Type
- Devices
View Company Profile
ID · c8fdfd28-35d5-4e17-aa2e-4023a75b11af
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 705331
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of FUJIFILM Healthcare Manufacturing Corporation, MIE Office
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 21, 2019 | Not classified | Office of Inspections and Investigations | |
| November 24, 2016 | Not classified | Office of Inspections and Investigations | |
| February 6, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 9, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for FUJIFILM Healthcare Manufacturing Corporation, MIE Office
- FDA Inspection 1136964 - 2019-06-21
- FDA Inspection 996390 - 2016-11-24
- FDA Inspection 869646 - 2014-02-06
- FDA Inspection 704811 - 2010-12-09
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