FDA Inspection 1113619 — Controltek, Inc.

Controltek, Inc. — FEI 3001452666

The FDA completed an inspection of Controltek, Inc. on December 20, 2019 in Vancouver, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 20, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Vancouver, WA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures