FDA Inspection 1091789 - Philips Medical Systems (Cleveland) Inc - June 04, 2019

FDA Inspection 1091789 for Philips Medical Systems (Cleveland) Inc on June 04, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1091789 for Philips Medical Systems (Cleveland) Inc on June 04, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(b)

21 CFR 820.198(a)

21 CFR 820.198(d)

21 CFR 820.40(a)

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Record Information

Company

Philips Medical Systems (Cleveland) Inc

Inspection Date

June 4, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 92f21a84-5876-4545-a688-e8cda0cbb583

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