FDA Inspection 1093409 — Urquima, Sa

Urquima, Sa — FEI 3002808432

The FDA completed an inspection of Urquima, Sa on September 21, 2017 in Sant Fost De Campsentelles. 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
September 21, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Fost De Campsentelles (Spain)

Additional Details

Mutual Recognition Agreement (MRA)