Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1950222.
Observations9
Issue DateJune 05, 2024
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
June 05, 2024
Country
United States
Inspection History, 2013 to 2026
VAI3
OAI7
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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