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 3004483441.
Observations3
Issue DateAugust 22, 2018
StatusNo Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections6
Establishment Details
Firm
Cantrell Drug Company
Location
Little Rock, Arkansas, United States
FEI Number
3004483441
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
August 22, 2018
Country
United States
Inspection History, 2011 to 2018
NAI1
VAI1
OAI4
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
Talk to a Specialist