# FDA Inspection 738991 - Tekia,  Inc. - August 04, 2011

Source: https://www.keypedia.com/records/fda_inspections/tekia-inc/46c25bf2-e930-4c49-843f-4af8cdbf4bac
Source feed: FDA_Inspections

> FDA Inspection 738991 for Tekia,  Inc. on August 04, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 738991
- Company Name: Tekia,  Inc.
- Inspection Date: 2011-08-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 738991 - 2011-08-04](https://www.keypedia.com/records/fda_inspections/tekia-inc/9cdd44ca-8077-4243-aeb5-d3a177ec010c)

Company: https://www.keypedia.com/companies/tekia-inc/4d9d4d15-c320-416e-8f73-9c178628a911

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