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FDA Inspection 851640 — Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.

Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. — FEI 1950222

The FDA completed an inspection of Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. on October 9, 2013 in Saint Louis, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 9, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)

Facility

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Recent compliance actions

FDA data resources