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FDA Inspection 634593 — Tutogen Medical GmbH

Tutogen Medical GmbH — FEI 3002924436

The FDA completed an inspection of Tutogen Medical GmbH on November 27, 2009 in Neunkirchen A. Brand. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 27, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Neunkirchen A. Brand (Germany)

Facility

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