FDA Inspection 1020883 — Spentech, Inc.

Spentech, Inc. — FEI 3003139439

The FDA completed an inspection of Spentech, Inc. on July 27, 2017 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 27, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Redmond, WA (United States)