FDA Inspection 862095 — Spectros Medical Devices Inc

Spectros Medical Devices Inc — FEI 3004957206

The FDA completed an inspection of Spectros Medical Devices Inc on January 15, 2014 in Houston, TX. 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
January 15, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, TX (United States)