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FDA Inspection 1007608 — 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 March 24, 2017 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
March 24, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)

Facility

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  • 919720 (VAI Mon Mar 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 902281 (OAI Tue Nov 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867214 (OAI Fri Feb 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources