# TEKNO MEDICAL OPTIK-CHIRURGIE GMBH – FDA Inspection, Dec 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/tekno-medical-optik-chirurgie-gmbh/18091e2e-8e01-4f8e-90f6-15da05b1e5da
Source feed: FDA_Inspections

> FDA inspection 1074283 of TEKNO MEDICAL OPTIK-CHIRURGIE GMBH, December 13, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074283
- Company Name: TEKNO MEDICAL OPTIK-CHIRURGIE GMBH
- Inspection Date: 2018-12-13
- 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: 2

## Related Documents

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- FDA Inspection 988493 - 2016-07-06
- FDA Inspection 843002 - 2013-07-25

## Related Officers

- [Company Rep](https://www.keypedia.com/people/yehualashet-a-gessesse/cb732900-358c-4982-a912-e98fa45142fe)

Company: https://www.keypedia.com/companies/tekno-medical-optik-chirurgie-gmbh/6268e4a6-3f54-4b12-8e27-c95f75fa478c

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