FDA Inspection 566225 — Vortran Medical Technology 1, Inc

Vortran Medical Technology 1, Inc — FEI 1000307109

The FDA completed an inspection of Vortran Medical Technology 1, Inc on February 26, 2009 in Sacramento, 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 26, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Sacramento, CA (United States)