FDA Inspection 1320930 — LSEHL

LSEHL — FEI 3013221811

The FDA completed an inspection of LSEHL on Jun 22, 2022 in Venissieux. 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
Jun 22, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Venissieux (France)

Additional Details

Mutual Recognition Agreement (MRA)