FDA issued a Warning Letter to Philips Medical Systems on 1/29/2007 for a previous inspection.
483 Philips Electronics North America Apr 2008

483 Philips Electronics North America Apr 2008

Dennis Kawabata FDA, Stephen Souza FDA$119.00 - Available Now

FDA investigators audited the Philips Electronics North America - Bothell, WA, United States facility and issued inspectional observations (via FDA 483) on 11 Apr 2008.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 11 Apr 2008
  • Location: Bothell, United States
  • FEI: 1000524572
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