FDA Inspection
FUJIFILM Healthcare Manufacturing Corporation, MIE OfficeFUJIFILM Healthcare Manufacturing Corporation, MIE Office – FDA Inspection, Jun 21, 2019
Record Details
This FDA Inspection record concerns FUJIFILM Healthcare Manufacturing Corporation, MIE Office, with an inspection on June 21, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- June 21, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 93f0f331-61d0-4b57-8897-5c5c0e0f8908
Inspection Facts
- Inspection number
- 1136964
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of FUJIFILM Healthcare Manufacturing Corporation, MIE Office
4| Date | Classification | Office | Project area |
|---|---|---|---|
| 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 |
| December 9, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for FUJIFILM Healthcare Manufacturing Corporation, MIE Office
- FDA Inspection 996390 - 2016-11-24
- FDA Inspection 869646 - 2014-02-06
- FDA Inspection 705331 - 2010-12-09
- FDA Inspection 704811 - 2010-12-09
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