# FDA Inspection 924751 - EndoChoice WCDC - April 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/endochoice-wcdc/04324abf-1268-4b32-b5a7-a8208b0c4027
Source feed: FDA_Inspections

> FDA Inspection 924751 for EndoChoice WCDC on April 30, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 924751
- Company Name: EndoChoice WCDC
- Inspection Date: 2015-04-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 924751 - 2015-04-30](https://www.keypedia.com/records/fda_inspections/endochoice-wcdc/75078622-dc4c-4f79-af90-3e089ebaee94)
- [FDA Inspection 830873 - 2013-05-08](https://www.keypedia.com/records/fda_inspections/endochoice-wcdc/451124db-231f-46bf-8457-30cb85847084)

Company: https://www.keypedia.com/companies/endochoice-wcdc/c7191acd-1c5b-436d-b909-f0f5e8ca8fa0

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