# FDA Inspection 1243511 - Ameritek USA, Inc. - July 10, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/ameritek-usa-inc/dffb32dc-4d28-4176-801d-66bc4bffc485
Source feed: FDA_Inspections

> FDA Inspection 1243511 for Ameritek USA, Inc. on July 10, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1243511
- Company Name: Ameritek USA, Inc.
- Inspection Date: 2024-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1243511 - 2024-07-10](https://www.globalkeysolutions.net/records/fda_inspections/ameritek-usa-inc/54c57803-b291-4b07-8a02-b937f265981b)
- [FDA Inspection 918166 - 2015-03-12](https://www.globalkeysolutions.net/records/fda_inspections/ameritek-usa-inc/417ac986-65a3-461f-a8da-86534e27de5e)
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- [FDA Inspection 799088 - 2012-09-17](https://www.globalkeysolutions.net/records/fda_inspections/ameritek-usa-inc/e8547246-bbda-405c-9904-6b4777d40235)
- [FDA Inspection 799088 - 2012-09-17](https://www.globalkeysolutions.net/records/fda_inspections/ameritek-usa-inc/ea7ee3d4-be0a-442f-bf2c-131ac2a61eb1)

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