FDA Inspection 1014715 — Laurimed LLC

Laurimed LLC — FEI 3007209822

The FDA completed an inspection of Laurimed LLC on May 16, 2017 in Redwood City, 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 16, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Redwood City, CA (United States)