FDA Inspection 770843 — Hollister Incorporated

Hollister Incorporated — FEI 1480288

The FDA completed an inspection of Hollister Incorporated on Mar 6, 2012 in Libertyville, IL. 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Libertyville, IL (United States)