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FDA Inspection 993103 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806559

The FDA completed an inspection of Roche Diagnostics GmbH on November 18, 2016 in Mannheim. 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 18, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mannheim (Germany)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 1177109 (VAI Fri Oct 29 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1103444 (VAI Thu Aug 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1057452 (NAI Thu Apr 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 973782 (NAI Fri Apr 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 928460 (NAI Wed May 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

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