FDA issued a Warning Letter to Philips Medical Systems on 1/29/2007 for a previous inspection.
483 Philips North America Dec 2018

483 Philips North America Dec 2018

Paul Kawamoto FDA, Phillip Pontikos FDA$119.00 - Available Now

FDA investigators audited the Philips North America - Bothell, WA, United States facility and issued inspectional observations (via FDA 483) on 03 Dec 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 03 Dec 2018
  • Location: Bothell, United States
  • FEI: 1000524572
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