FDA Inspection 1100060 - Eisertech LLC - August 21, 2019

FDA Inspection 1100060 for Eisertech LLC on August 21, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1100060 for Eisertech LLC on August 21, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Eisertech LLC

Inspection Date

August 21, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fed9d684-55ec-46e1-a341-0849b7737d90

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