FDA Inspection 993016 - Bauerfeind AG - November 04, 2016

FDA Inspection 993016 for Bauerfeind AG on November 04, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 993016 for Bauerfeind AG on November 04, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Bauerfeind AG

Inspection Date

November 4, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9b5a6cf-b414-42e1-9534-9699e6d8057c

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