FDA Inspection 960010 — Eurofins Advantar Laboratories, LLC

Eurofins Advantar Laboratories, LLC — FEI 3007801780

The FDA completed an inspection of Eurofins Advantar Laboratories, LLC on February 3, 2016 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 3, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
San Diego, CA (United States)