# FDA Inspection 1262494 - CAMNTECH - January 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/camntech/06a0b1df-ee93-4005-9f33-f49fb87656d3
Source feed: FDA_Inspections

> FDA Inspection 1262494 for CAMNTECH on January 16, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1262494
- Company Name: CAMNTECH
- Inspection Date: 2025-01-16
- 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 1262494 - 2025-01-16](https://www.keypedia.com/records/fda_inspections/camntech/f49a150c-267b-4427-b891-46b48b350218)
- [FDA Inspection 1262494 - 2025-01-16](https://www.keypedia.com/records/fda_inspections/camntech/24b20645-f36c-4587-94d7-5622e4dd99ba)
- [FDA Inspection 1020179 - 2017-08-03](https://www.keypedia.com/records/fda_inspections/camntech/5c847ef0-6baa-4384-80fd-c54c3a9a7a8b)

Company: https://www.keypedia.com/companies/camntech/5a2bcf5a-6123-4b31-93f0-4ee95cfa86a2

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