FDA Inspection 946520 — Cramer Products Inc

Cramer Products Inc — FEI 1910082

The FDA completed an inspection of Cramer Products Inc on October 26, 2015 in Gardner, KS. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 26, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Gardner, KS (United States)