FDA Inspection
FUJIFILM Healthcare Manufacturing Corporation, MIE OfficeFDA Inspection 705331 - FUJIFILM Healthcare Manufacturing Corporation, MIE Office - December 09, 2010
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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
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ID · c8fdfd28-35d5-4e17-aa2e-4023a75b11af