FDA Inspection 1034925 — Microgen Bioproducts Limited

Microgen Bioproducts Limited — FEI 1000234991

The FDA completed an inspection of Microgen Bioproducts Limited on May 10, 2017 in Camberley. 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
May 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Camberley (United Kingdom)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation
337521 CFR 820.198(e)Records of complaint investigation
369621 CFR 820.100(b)Documentation