FDA Inspection 1054311 - Karl Storz Endoscopy - April 16, 2018
FDA Inspection 1054311 for Karl Storz Endoscopy on April 16, 2018. Classification: No Action Indicated (NAI).
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FDA Inspection 1054311 for Karl Storz Endoscopy on April 16, 2018. Classification: No Action Indicated (NAI).
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Company
Karl Storz EndoscopyInspection Date
April 16, 2018
Product Type
Devices
ID: fdf48c33-627a-4c0f-8ce9-6070433db16d
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