Source: FDA record for this establishment. FDA 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1950222.
Observations3
Issue DateJuly 31, 2009
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
Location
Saint Louis, Missouri, United States
FEI Number
1950222
Product Type
Drugs
Issue Date
July 31, 2009
Country
United States
Inspection History, 2013 to 2026
VAI3
OAI7
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.