FDA Inspection 945848 - Evergreen Orthopedic Research Lab, LLC dba Opertiv - October 29, 2015
FDA Inspection 945848 for Evergreen Orthopedic Research Lab, LLC dba Opertiv on October 29, 2015. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 945848 for Evergreen Orthopedic Research Lab, LLC dba Opertiv on October 29, 2015. Classification: Voluntary Action Indicated (VAI).
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Inspection Date
October 29, 2015
Product Type
Devices
ID: fa031fe5-a19d-4a63-8af8-1f681c810d62
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