FDA Inspection 924146 — Interlabor Belp Ag

Interlabor Belp Ag — FEI 3001264559

The FDA completed an inspection of Interlabor Belp Ag on Apr 24, 2015 in Belp. 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
Apr 24, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Belp (Switzerland)