FDA Inspection 1022578 - Philips Medical Systems (Cleveland) Inc - August 18, 2017

FDA Inspection 1022578 for Philips Medical Systems (Cleveland) Inc on August 18, 2017. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1022578 for Philips Medical Systems (Cleveland) Inc on August 18, 2017. Classification: Official Action Indicated (OAI).

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Record Information

Company

Philips Medical Systems (Cleveland) Inc

Inspection Date

August 18, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 583923d3-73de-474b-9d1f-43276227f96d

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