Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1950222.
Observations9
Issue DateJuly 24, 2015
StatusNo Warning Letter
Establishment TypePharmaceutical Manufacturer
Related Inspections10
Establishment Details
Firm
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
Issued To
Meridian Medical Technologies a Pfizer Company
Location
Saint Louis, Missouri, United States
FEI Number
1950222
Establishment Type
Pharmaceutical Manufacturer
Product Type
Drugs
Issue Date
July 24, 2015
Country
United States
Inspection History, 2013 to 2026
VAI3
OAI7
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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