FDA Inspection 1036375 — Hollister Incorporated

Hollister Incorporated — FEI 1480288

The FDA completed an inspection of Hollister Incorporated on Dec 19, 2017 in Libertyville, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 19, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Libertyville, IL (United States)