FDA Inspection 1080989 - Rachel L. Moore, M.D. - February 21, 2019

FDA Inspection 1080989 for Rachel L. Moore, M.D. on February 21, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1080989 for Rachel L. Moore, M.D. on February 21, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Rachel L. Moore, M.D.

Inspection Date

February 21, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f86bf816-9617-4694-a716-eeb7e2c5d752

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