JK Products & Services, Inc

Form 483

Jonesboro, Arkansas, United StatesFEI 2311923Issued February 10, 2012

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 2311923.

Observations11

Issue DateFebruary 10, 2012

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: JK Products & Services, Inc
Location: Jonesboro, Arkansas, United States
FEI Number: 2311923
Product Type: Devices
Issue Date: February 10, 2012
Country: United States

Inspection History, 2010 to 2017

NAI2

VAI3

NAI means No Action Indicated. VAI means Voluntary 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.

JK Products & Services, Inc FDA Form 483, Jonesboro, Arkansas, February 10, 2012