# Cortek Endoscopy Inc – FDA Inspection, Jun 16, 2015

Source: https://www.keypedia.com/records/fda_inspections/cortek-endoscopy-inc/735ec183-266a-419c-8758-bdf16b5ac5cd
Source feed: FDA_Inspections

> FDA inspection 930407 of Cortek Endoscopy Inc, June 16, 2015. Classification: Voluntary Action Indicated (VAI). 3 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: 930407
- Company Name: Cortek Endoscopy Inc
- Inspection Date: 2015-06-16
- 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: 3

## Related Documents

- [FDA Inspection 1069062 - 2018-10-16](https://www.keypedia.com/records/fda_inspections/cortek-endoscopy-inc/c108a560-6ede-43b7-b320-80ad6f7ac4e3)
- [FDA Inspection 739709 - 2011-08-16](https://www.keypedia.com/records/fda_inspections/cortek-endoscopy-inc/bbc8253d-cb37-414a-957e-d3bbc4873602)

Company: https://www.keypedia.com/companies/cortek-endoscopy-inc/c3f13b8b-0b84-4fc3-b085-250878922ace

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