# Tekna Manufacturing, LLC – FDA Inspection, Apr 29, 2014

Source: https://www.keypedia.com/records/fda_inspections/tekna-manufacturing-llc/c2adb2b8-5650-4c10-b833-53929c747b98
Source feed: FDA_Inspections

> FDA inspection 876586 of Tekna Manufacturing, LLC, April 29, 2014. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 876586
- Company Name: Tekna Manufacturing, LLC
- Inspection Date: 2014-04-29
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1006295 - 2017-02-28](https://www.keypedia.com/records/fda_inspections/tekna-manufacturing-llc/9b704082-c347-4572-9069-cd2aa57cce59)
- [FDA Inspection 841403 - 2013-07-22](https://www.keypedia.com/records/fda_inspections/tekna-manufacturing-llc/b2a5712f-4057-4eb9-a6e4-955802d48960)

Company: https://www.keypedia.com/companies/tekna-manufacturing-llc/277c82c2-433a-4158-ba25-a197d328f702

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