FDA Inspection 1023770 — Avazzia, Inc

Avazzia, Inc — FEI 3004839404

The FDA completed an inspection of Avazzia, Inc on August 30, 2017 in Dallas, TX. 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
August 30, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Dallas, TX (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures