FDA Inspection 870293 — Atossa Genetics, Inc.

Atossa Genetics, Inc. — FEI 3009171441

The FDA completed an inspection of Atossa Genetics, Inc. on March 14, 2014 in Seattle, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 14, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Seattle, WA (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures