FDA Inspection 988709 — Phyton Biotech GmbH

Phyton Biotech GmbH — FEI 3002807883

The FDA completed an inspection of Phyton Biotech GmbH on July 15, 2016 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
July 15, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ahrensburg (Germany)