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FDA Inspection 635560 — Rommelag CDMO GmbH

Rommelag CDMO GmbH — FEI 3002808845

The FDA completed an inspection of Rommelag CDMO GmbH on November 19, 2009 in Sulzbach-Laufen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 19, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Sulzbach-Laufen (Germany)

Facility

Other inspections at this facility

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  • 1118070 (NAI Tue Feb 18 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1107432 (NAI Tue Sep 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949464 (VAI Thu Oct 22 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 880428 (VAI Fri Feb 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

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