# FDA Inspection 1175910 - Aomori Olympus Co., Ltd. - July 14, 2022

Source: https://www.keypedia.com/records/fda_inspections/aomori-olympus-co-ltd/03ada651-d95a-48b2-bfd1-c9af414fb5cb
Source feed: FDA_Inspections

> FDA Inspection 1175910 for Aomori Olympus Co., Ltd. on July 14, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1175910
- Company Name: Aomori Olympus Co., Ltd.
- Inspection Date: 2022-07-14
- Classification: Voluntary Action Indicated (VAI)
- 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
