FDA Inspection 1069935 — Follett LLC

Follett LLC — FEI 3012660965

The FDA completed an inspection of Follett LLC on Oct 25, 2018 in Bethlehem, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 25, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Bethlehem, PA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.