Home / Inspections / 1048872

FDA Inspection 1048872 — Tutogen Medical GmbH

Tutogen Medical GmbH — FEI 3002924436

The FDA completed an inspection of Tutogen Medical GmbH on March 8, 2018 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
March 8, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Neunkirchen A. Brand (Germany)

Facility

Other inspections at this facility

  • 1325500 (NAI Thu Jun 25 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1220073 (NAI Thu Aug 31 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 943795 (NAI Wed Sep 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 815199 (NAI Fri Jan 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 634593 (NAI Fri Nov 27 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources