# FDA Inspection 960600 - Aomori Olympus Co., Ltd. - March 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/aomori-olympus-co-ltd/56b9e481-cf52-4ed0-9245-ac395e105422
Source feed: FDA_Inspections

> FDA Inspection 960600 for Aomori Olympus Co., Ltd. on March 02, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960600
- Company Name: Aomori Olympus Co., Ltd.
- Inspection Date: 2016-03-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/aomori-olympus-co-ltd/0ed7e8a7-97a2-425f-8c57-6d32c40902c4

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