# FDA Inspection 1211356 - Fettech - July 14, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/fettech/dd6c8416-7dea-4eea-8d0d-f9d585764972
Source feed: FDA_Inspections

> FDA Inspection 1211356 for Fettech on July 14, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1211356
- Company Name: Fettech
- Inspection Date: 2023-07-14
- 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 1299534 - 2025-12-16](https://www.globalkeysolutions.net/records/fda_inspections/fettech/7a470f45-15d0-47f7-a0c7-6917d05d2909)
- [FDA Inspection 1299534 - 2025-12-16](https://www.globalkeysolutions.net/records/fda_inspections/fettech/1bc9855e-93ab-48e4-88dc-aa8a77950df0)
- [FDA Inspection 1299534 - 2025-12-16](https://www.globalkeysolutions.net/records/fda_inspections/fettech/ab16dc5f-eb52-49f7-a4fd-6673ef4108a1)
- [FDA Inspection 1211356 - 2023-07-14](https://www.globalkeysolutions.net/records/fda_inspections/fettech/76def794-b827-4c2e-ad19-87d7313d4b97)

Company: https://www.globalkeysolutions.net/companies/fettech/c0f3a2f5-d032-4c6c-8389-066f9e8e6c76

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