FDA Inspection 990064 — Urquima, Sa

Urquima, Sa — FEI 3002808432

The FDA completed an inspection of Urquima, Sa on Sep 29, 2016 in Sant Fost De Campsentelles. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 29, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Fost De Campsentelles (Spain)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.