Cantrell Drug Company

Form 483

Little Rock, Arkansas, United StatesFEI 3004483441Issued June 29, 2017

View FDA's Record for This Firm

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 3004483441.

Observations8

Issue DateJune 29, 2017

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Cantrell Drug Company
Location: Little Rock, Arkansas, United States
FEI Number: 3004483441
Product Type: Drugs
Issue Date: June 29, 2017
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.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Cantrell Drug Company FDA Form 483, Little Rock, Arkansas, June 29, 2017