# Ameritek USA, Inc. – FDA Inspection, Sep 8, 2010

Source: https://www.keypedia.com/records/fda_inspections/ameritek-usa-inc/121463c7-fdf1-4af3-b3be-e43eb75fe122
Source feed: FDA_Inspections

> FDA inspection 682875 of Ameritek USA, Inc., September 08, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 682875
- Company Name: Ameritek USA, Inc.
- Inspection Date: 2010-09-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1243511 - 2024-07-10](https://www.keypedia.com/records/fda_inspections/ameritek-usa-inc/dffb32dc-4d28-4176-801d-66bc4bffc485)
- FDA Inspection 918166 - 2015-03-12
- FDA Inspection 799088 - 2012-09-17

Company: https://www.keypedia.com/companies/ameritek-usa-inc/62a3cc23-623b-4822-a265-a6773e3ccd01

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