FDA Inspection 878312 — Covis Pharma GmBH

Covis Pharma GmBH — FEI 3008152278

The FDA completed an inspection of Covis Pharma GmBH on May 21, 2014 in Waltham, MA. 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
May 21, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Waltham, MA (United States)