FDA Inspection 949462 — LumiQuick Diagnostics Inc.
The FDA completed an inspection of LumiQuick Diagnostics Inc. on November 17, 2015 in Santa Clara, 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
- November 17, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Santa Clara, CA (United States)