FDA Inspection 549341 — Stericycle, Inc.

Stericycle, Inc. — FEI 3004714969

The FDA completed an inspection of Stericycle, Inc. on Nov 7, 2008 in Lakeland, FL. 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
Nov 7, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lakeland, FL (United States)