FDA issued a Warning Letter to Roche Diagnostics Corporation on 9/2/2004 for a previous inspection.
483 Roche Diagnostics Aug 2016

483 Roche Diagnostics Aug 2016

Kennita Riddick FDA, Joseph Strelnik FDA$595.00 - Available Now

FDA investigators audited the Roche Diagnostics - Indianapolis, IN, United States facility and issued inspectional observations (via FDA 483) on 15 Aug 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 15 Aug 2016
  • Location: Indianapolis, United States
  • FEI: 1823260
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