FDA Inspection 631017 — HP Halden Pharma AS

HP Halden Pharma AS — FEI 3002608066

The FDA completed an inspection of HP Halden Pharma AS on November 17, 2009 in Halden. 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
November 17, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Halden (Norway)