FDA Inspection 1195599 - PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - January 26, 2023

FDA Inspection 1195599 for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. on January 26, 2023. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1195599 for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. on January 26, 2023. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 806.10(b)

21 CFR 820.160(a)

21 CFR 820.198(c)

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Record Information

Company

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Inspection Date

January 26, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fba9a565-7d32-4027-8268-68c6690852c3

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