FDA Inspection 850016 — Acro Biotech Inc.
The FDA completed an inspection of Acro Biotech Inc. on Sep 3, 2013 in Rancho Cucamonga, CA. 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
- Sep 3, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rancho Cucamonga, CA (United States)