FDA Inspection 1172729 — Acon Laboratories, Inc.

Acon Laboratories, Inc. — FEI 3003516723

The FDA completed an inspection of Acon Laboratories, Inc. on May 10, 2022 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
May 10, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)