FDA Inspection 1178993 — Temmler Pharma GmbH & Co. KG

Temmler Pharma GmbH & Co. KG — FEI 3002808339

The FDA completed an inspection of Temmler Pharma GmbH & Co. KG on September 16, 2020 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
September 16, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Marburg (Germany)

Additional Details

Mutual Recognition Agreement (MRA)