FDA Inspection 1068498 — Curexa - East, LLC dba Curexa

Curexa - East, LLC dba Curexa — FEI 3011761882

The FDA completed an inspection of Curexa - East, LLC dba Curexa on August 31, 2018 in Egg Harbor Township, NJ. 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
August 31, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Egg Harbor Township, NJ (United States)