FDA Inspection 966845 — Follett, LLC

Follett, LLC — FEI 3005883510

The FDA completed an inspection of Follett, LLC on March 29, 2016 in Easton, PA. 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
March 29, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Easton, PA (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained