FDA Inspection 670945 — Aaren Laboratories LLC

Aaren Laboratories LLC — FEI 3013202565

The FDA completed an inspection of Aaren Laboratories LLC on July 6, 2010 in Ontario, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 6, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Ontario, CA (United States)