FDA Inspection 722239 — Cayman Pharma s.r.o.

Cayman Pharma s.r.o. — FEI 3003625059

The FDA completed an inspection of Cayman Pharma s.r.o. on March 17, 2011 in Neratovice. 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 17, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Neratovice (Czech Republic)