FDA Inspection 995051 — Fundus Photo, LLC

Fundus Photo, LLC — FEI 3007237389

The FDA completed an inspection of Fundus Photo, LLC on December 21, 2016 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 21, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
313021 CFR 820.100(a)Lack of or inadequate procedures
333121 CFR 820.181DMR - not or inadequately maintained
334321 CFR 820.198(e)Maintained
341521 CFR 820.22Quality Audit/Reaudit - conducted
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures