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FDA Inspection
•FUJIFILM Healthcare Manufacturing Corp.•December 14, 2016

FUJIFILM Healthcare Manufacturing Corp. – FDA Inspection, Dec 14, 2016

Record Details

This FDA Inspection record concerns FUJIFILM Healthcare Manufacturing Corp., with an inspection on December 14, 2016, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
FUJIFILM Healthcare Manufacturing Corp.
Inspection Date
December 14, 2016
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Brian S. Keefer (FDA Associated Person)
View Company Profile

ID · ee638b84-0917-47da-b6f8-4cd6e8290052

Inspection Facts

Inspection number
996016
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of FUJIFILM Healthcare Manufacturing Corp.

2
DateClassificationOfficeProject area
March 10, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
February 19, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for FUJIFILM Healthcare Manufacturing Corp.
  • FDA Inspection 1200950 - 2023-03-10
  • FDA Inspection 870122 - 2014-02-19

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