FDA Inspection 852302 — ARP Wave L.L.C.
The FDA completed an inspection of ARP Wave L.L.C. on Oct 23, 2013 in Apple Valley, MN. 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
- Oct 23, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Apple Valley, MN (United States)