FDA Inspection 1042012 - EyeKon Medical, Inc. - February 16, 2018
FDA Inspection 1042012 for EyeKon Medical, Inc. on February 16, 2018. Classification: No Action Indicated (NAI).
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FDA Inspection 1042012 for EyeKon Medical, Inc. on February 16, 2018. Classification: No Action Indicated (NAI).
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Company
EyeKon Medical, Inc.Inspection Date
February 16, 2018
Product Type
Devices
ID: f8eb3c98-24c1-4465-b252-9ef6eda8161c
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