FDA Inspection 1121737 — Luye Pharma AG

Luye Pharma AG — FEI 3007515173

The FDA completed an inspection of Luye Pharma AG on July 9, 2019 in Miesbach. 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
July 9, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Miesbach (Germany)

Additional Details

Mutual Recognition Agreement (MRA)