FDA Inspection
Ameritek USA, Inc.Ameritek USA, Inc. – FDA Inspection, Jul 10, 2024
Record Details
This FDA Inspection record concerns Ameritek USA, Inc., with an inspection on July 10, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · dffb32dc-4d28-4176-801d-66bc4bffc485
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1243511
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Ameritek USA, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 12, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 17, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 8, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Ameritek USA, Inc.
- FDA Inspection 918166 - 2015-03-12
- FDA Inspection 799088 - 2012-09-17
- FDA Inspection 682875 - 2010-09-08
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