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FDA Inspection
•PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.•October 6, 2017

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. – FDA Inspection, Oct 6, 2017

Record Details

This FDA Inspection record concerns PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., with an inspection on October 6, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Inspection Date
October 6, 2017
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
View Company Profile

ID · eab253af-122a-4974-9614-14f151b56a5a

Inspection Facts

Inspection number
1047647
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

5
DateClassificationOfficeProject area
January 17, 2025OAICenter for Devices and Radiological HealthCompliance: Devices
January 26, 2023OAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
September 28, 2018Not classifiedOffice of Inspections and Investigations
September 21, 2010NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
November 20, 2008VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
  • FDA Inspection 1259266 - 2025-01-17
  • FDA Inspection 1195599 - 2023-01-26
  • FDA Inspection 1120490 - 2018-09-28
  • FDA Inspection 680386 - 2010-09-21
  • FDA Inspection 551807 - 2008-11-20

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