# FDA Inspection 704811 - FUJIFILM Healthcare Manufacturing Corporation, MIE Office - December 09, 2010

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-mie-office/b3dbd2c2-6684-4de4-98ac-81fa4a5705f4
Source feed: FDA_Inspections

> FDA Inspection 704811 for FUJIFILM Healthcare Manufacturing Corporation, MIE Office on December 09, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 704811
- Company Name: FUJIFILM Healthcare Manufacturing Corporation, MIE Office
- Inspection Date: 2010-12-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [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 705331 - 2010-12-09](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-mie-office/c8fdfd28-35d5-4e17-aa2e-4023a75b11af)

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