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Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. Form 483 Details

Form 483
Find this 483 on FDA
Source: FDA Data DashboardFDA has published this inspection and the number of observations cited. The form itself has not been released yet, which usually takes six to twelve months.
Check this firm on FDA, establishment 1950222

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

Saint Louis, Missouri, United States
Issue DateDecember 21, 2019
FEI Number1950222
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. FDA Form 483, Saint Louis, Missouri, December 21, 2019