# American Imex – FDA Inspection, Jan 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/american-imex/be895fb3-268e-48b6-8580-9cda40f4e0a5
Source feed: FDA_Inspections

> FDA inspection 958092 of American Imex, January 20, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 927130 - 2015-05-18](https://www.keypedia.com/records/fda_inspections/american-imex/c211a0c8-67b0-47c4-a206-f399d4265d12)
- FDA Inspection 758825 - 2011-12-16

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