FDA Inspection 1063743 - Amann Girrbach North America, L.P. - August 29, 2018

FDA Inspection 1063743 for Amann Girrbach North America, L.P. on August 29, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1063743 for Amann Girrbach North America, L.P. on August 29, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Amann Girrbach North America, L.P.

Inspection Date

August 29, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc66fff3-4929-451e-908c-1d1f4d944e71

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