FDA Inspection 1032165 — Contech Medical, Inc.

Contech Medical, Inc. — FEI 1221541

The FDA completed an inspection of Contech Medical, Inc. on November 17, 2017 in Providence, RI. 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
November 17, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Providence, RI (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures