Veru Inc. – FDA Inspection, Oct 20, 2016

Record Details

This FDA Inspection record concerns Veru Inc., with an inspection on October 20, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Veru Inc.
Inspection Date: October 20, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Jesse A. Vazquez (FDA Associated Person)

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ID · b2c9608e-db6f-4c36-8ec3-24e48c2d1932

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 993531
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices
Outcome: Form 483 issued

FDA Citations

21 CFR 820.20(a)Management ensuring quality policy is understood

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FDA Inspection

Veru Inc.October 20, 2016