FDA Inspection 918661 — Aurora Pharmaceutical, Inc.

Aurora Pharmaceutical, Inc. — FEI 3008276347

The FDA completed an inspection of Aurora Pharmaceutical, Inc. on Mar 19, 2015 in Northfield, MN. 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: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 19, 2015
Fiscal Year
2015
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Northfield, MN (United States)

Citations

IDCFRDescription
360321 CFR 211.160(b)Scientifically sound laboratory controls