FDA Inspection 670945 — Aaren Laboratories LLC

Aaren Laboratories LLC — FEI 3013202565

The FDA completed an inspection of Aaren Laboratories LLC on Jul 6, 2010 in Ontario, CA. 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
Jul 6, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Ontario, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.