FDA Inspection 965131 — Elorac Inc.

Elorac Inc. — FEI 3008393397

The FDA completed an inspection of Elorac Inc. on March 28, 2016 in Vernon Hills, IL. 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
March 28, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Vernon Hills, IL (United States)