FDA Inspection 819228 — Lusys Laboratories, Inc.

Lusys Laboratories, Inc. — FEI 3004473533

The FDA completed an inspection of Lusys Laboratories, Inc. on February 21, 2013 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
February 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)