# FDA Inspection 978631 - EpiEP, Inc. - July 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/epiep-inc/908c8e0f-291e-44b9-ad59-df8529737b22
Source feed: FDA_Inspections

> FDA Inspection 978631 for EpiEP, Inc. on July 07, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 978631
- Company Name: EpiEP, Inc.
- Inspection Date: 2016-07-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/epiep-inc/86a3fbf3-f101-4646-a2bb-5425e63eb1de

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