# FDA Inspection 1101763 - ATEK Manufacturing - July 02, 2019

Source: https://www.keypedia.com/records/fda_inspections/atek-manufacturing/f2d4c753-5522-4ff5-9bfa-dd65751b4d3e
Source feed: FDA_Inspections

> FDA Inspection 1101763 for ATEK Manufacturing on July 02, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101763
- Company Name: ATEK Manufacturing
- Inspection Date: 2019-07-02
- 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 1101763 - 2019-07-02](https://www.keypedia.com/records/fda_inspections/atek-manufacturing/31b20e7d-db06-4d6e-bba2-f4d21f163e3c)

Company: https://www.keypedia.com/companies/atek-manufacturing/52dbeae5-75c2-41b4-bf4a-86a100f833ab

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