FDA Inspection 936431 - Renfro Corporation - June 16, 2015
FDA Inspection 936431 for Renfro Corporation on June 16, 2015. Classification: No Action Indicated (NAI).
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FDA Inspection 936431 for Renfro Corporation on June 16, 2015. Classification: No Action Indicated (NAI).
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Company
Renfro CorporationInspection Date
June 16, 2015
Product Type
Devices
ID: f71fadc4-d198-4498-afa2-31c42092abc0
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