Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. Form 483 Details
Form 483Source: FDA record for this establishmentFDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 1950222.
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
Saint Louis, Missouri, United States
Issue DateFebruary 13, 2012
FEI Number1950222
CountryUnited States
Status
No Warning LetterProduct Type
Drugs