FDA Inspection 1059989 — Altaravision, Inc.
The FDA completed an inspection of Altaravision, Inc. on March 20, 2018 in Apex, NC. 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
- March 20, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Apex, NC (United States)