# FDA Inspection 958092 - American Imex - January 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/american-imex/3e27607b-c73f-47d6-bc7a-90f2a0ce0b34
Source feed: FDA_Inspections

> FDA Inspection 958092 for American Imex on January 20, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 958092
- Company Name: American Imex
- Inspection Date: 2016-01-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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Company: https://www.keypedia.com/companies/american-imex/b509b173-db68-45c8-a536-d5f67ea4bd83

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