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FDA Inspection 867214 — 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 February 21, 2014 in Saint Louis, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 21, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)

Facility

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Recent compliance actions

FDA data resources