FDA Inspection 1069143 — Apex360, LLC
The FDA completed an inspection of Apex360, LLC on October 17, 2018 in Burlington, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- October 17, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Burlington, KY (United States)