FDA Inspection 833099 — Epigenomics Ag

Epigenomics Ag — FEI 3005968611

The FDA completed an inspection of Epigenomics Ag on May 24, 2013 in Berlin. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 24, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Berlin (Germany)