FDA Inspection 959093 - Degania Medical Devices Pvt. Ltd. - January 21, 2016

FDA Inspection 959093 for Degania Medical Devices Pvt. Ltd. on January 21, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 959093 for Degania Medical Devices Pvt. Ltd. on January 21, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Degania Medical Devices Pvt. Ltd.

Inspection Date

January 21, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 0e795dae-2c19-4553-966b-7ff8071b9073

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