# FUJIFILM Healthcare Manufacturing Corporation, MIE Office – FDA Inspection, Dec 9, 2010

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-mie-office/c8fdfd28-35d5-4e17-aa2e-4023a75b11af
Source feed: FDA_Inspections

> FDA inspection 705331 of FUJIFILM Healthcare Manufacturing Corporation, MIE Office, December 09, 2010. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 705331
- Company Name: FUJIFILM Healthcare Manufacturing Corporation, MIE Office
- Inspection Date: 2010-12-09
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1136964 - 2019-06-21](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-mie-office/93f0f331-61d0-4b57-8897-5c5c0e0f8908)
- FDA Inspection 996390 - 2016-11-24
- [FDA Inspection 869646 - 2014-02-06](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-mie-office/394fcfbd-9bac-446c-b2e2-a636cebba455)
- FDA Inspection 704811 - 2010-12-09

Company: https://www.keypedia.com/companies/fujifilm-healthcare-manufacturing-corporation-mie-office/05242525-4bc7-4608-8dad-c9d76d7c69a2

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7