FDA Inspection 917700 - Michael Caplan, MD - February 25, 2015
FDA Inspection 917700 for Michael Caplan, MD on February 25, 2015. Classification: No Action Indicated (NAI).
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FDA Inspection 917700 for Michael Caplan, MD on February 25, 2015. Classification: No Action Indicated (NAI).
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Michael Caplan, MDInspection Date
February 25, 2015
Product Type
Devices
ID: fc79c823-605e-4a9c-91af-3ba13a010ad3
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