FDA Inspection 1000177 — Phytolab Gmbh & Co KG

Phytolab Gmbh & Co KG — FEI 3003204295

The FDA completed an inspection of Phytolab Gmbh & Co KG on January 10, 2017 in Vestenbergsgreuth. 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
January 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vestenbergsgreuth (Germany)