FDA Inspection 611081 — HTL

HTL — FEI 3006408331

The FDA completed an inspection of HTL on Jun 19, 2009 in Javene. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 19, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Javene (France)