FDA Inspection 894933 — GEODIS C/O PUREFRUIT/ TOPCO

GEODIS C/O PUREFRUIT/ TOPCO — FEI 3016704096

The FDA completed an inspection of GEODIS C/O PUREFRUIT/ TOPCO on September 10, 2014 in Joliet, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 10, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Joliet, IL (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained