FDA Inspection 886820 - Koning Corporation - July 08, 2014
FDA Inspection 886820 for Koning Corporation on July 08, 2014. Classification: No Action Indicated (NAI).
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FDA Inspection 886820 for Koning Corporation on July 08, 2014. Classification: No Action Indicated (NAI).
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Company
Koning CorporationInspection Date
July 8, 2014
Product Type
Devices
ID: e0f0d32f-1d1d-4cdc-ae94-5c250fc88acd
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