FDA Inspection 1132948 — Phyton Biotech GmbH

Phyton Biotech GmbH — FEI 3002807883

The FDA completed an inspection of Phyton Biotech GmbH on February 20, 2020 in Ahrensburg. 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
February 20, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ahrensburg (Germany)

Additional Details

Mutual Recognition Agreement (MRA)