# FDA Inspection 930407 - Cortek Endoscopy Inc - June 16, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/cortek-endoscopy-inc/49c49183-39c2-4c57-8e9c-5db0bea334ca
Source feed: FDA_Inspections

> FDA Inspection 930407 for Cortek Endoscopy Inc on June 16, 2015. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1069062 - 2018-10-16](https://www.globalkeysolutions.net/records/fda_inspections/cortek-endoscopy-inc/c108a560-6ede-43b7-b320-80ad6f7ac4e3)
- [FDA Inspection 1069062 - 2018-10-16](https://www.globalkeysolutions.net/records/fda_inspections/cortek-endoscopy-inc/5ecbc77c-37d0-4e51-8abf-1fa0e9b46a3a)
- [FDA Inspection 930407 - 2015-06-16](https://www.globalkeysolutions.net/records/fda_inspections/cortek-endoscopy-inc/735ec183-266a-419c-8758-bdf16b5ac5cd)
- [FDA Inspection 739709 - 2011-08-16](https://www.globalkeysolutions.net/records/fda_inspections/cortek-endoscopy-inc/bbc8253d-cb37-414a-957e-d3bbc4873602)
- [FDA Inspection 739709 - 2011-08-16](https://www.globalkeysolutions.net/records/fda_inspections/cortek-endoscopy-inc/384d1c64-50be-4b87-a60d-5d3f518ace7b)

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

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