FDA Inspection 902281 - Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. - November 25, 2014
FDA Inspection 902281 for Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. on November 25, 2014. Classification: Official Action Indicated (OAI).
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FDA Inspection 902281 for Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. on November 25, 2014. Classification: Official Action Indicated (OAI).
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Inspection Date
November 25, 2014
Product Type
Devices
ID: f7d3054f-efae-48ad-a913-5d706dfd39e3
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