FDA Inspection 993531 — Veru Inc.

Veru Inc. — FEI 1000515210

The FDA completed an inspection of Veru Inc. on Oct 20, 2016 in Miami, FL. 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 20, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)

Citations

IDCFRDescription
405721 CFR 820.20(a)Management ensuring quality policy is understood