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FDA Inspection 919720 — 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 23, 2015 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 23, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)

Facility

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  • 1007608 (OAI Fri Mar 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
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Recent compliance actions

FDA data resources