FDA Inspection 1002547 — ARP Wave L.L.C.
The FDA completed an inspection of ARP Wave L.L.C. on Feb 7, 2017 in Apple Valley, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Feb 7, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Apple Valley, MN (United States)