FDA Inspection 788609 — Temmler Pharma GmbH & Co. KG

Temmler Pharma GmbH & Co. KG — FEI 3002808339

The FDA completed an inspection of Temmler Pharma GmbH & Co. KG on June 22, 2012 in Marburg. 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
June 22, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Marburg (Germany)