# Tekna Manufacturing, LLC – FDA Inspection, Jul 22, 2013

Source: https://www.keypedia.com/records/fda_inspections/tekna-manufacturing-llc/b2a5712f-4057-4eb9-a6e4-955802d48960
Source feed: FDA_Inspections

> FDA inspection 841403 of Tekna Manufacturing, LLC, July 22, 2013. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 841403
- Company Name: Tekna Manufacturing, LLC
- Inspection Date: 2013-07-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## 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 876586 - 2014-04-29](https://www.keypedia.com/records/fda_inspections/tekna-manufacturing-llc/c2adb2b8-5650-4c10-b833-53929c747b98)

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