# FDA Inspection 682875 - Ameritek USA, Inc. - September 08, 2010

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

> FDA Inspection 682875 for Ameritek USA, Inc. on September 08, 2010. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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