FDA Inspection 775766 — VicTorch Meditek, Inc

VicTorch Meditek, Inc — FEI 3003323921

The FDA completed an inspection of VicTorch Meditek, Inc on March 19, 2012 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
March 19, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)