FDA Inspection 735761 — Spentech, Inc.

Spentech, Inc. — FEI 3003139439

The FDA completed an inspection of Spentech, Inc. on July 21, 2011 in Redmond, WA. 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
July 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Redmond, WA (United States)