FDA Inspection 978631 — EpiEP, Inc.
The FDA completed an inspection of EpiEP, Inc. on Jul 7, 2016 in Blue Ash, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 7, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Blue Ash, OH (United States)