FDA Inspection 970553 — Acon Laboratories, Inc.
The FDA completed an inspection of Acon Laboratories, Inc. on April 15, 2016 in San Diego, CA. 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
- April 15, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- San Diego, CA (United States)