FDA Inspection 662439 — Nycomed Gmbh

Nycomed Gmbh — FEI 3007686024

The FDA completed an inspection of Nycomed Gmbh on Apr 24, 2010 in Konstanz. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 24, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Konstanz (Germany)

Additional details

Sponsor, Contract Research Organization

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