Neurolumen LLC

Form 483

Oklahoma City, Oklahoma, United StatesFEI 3010144038Issued May 08, 2015

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 3010144038.

Observations10

Issue DateMay 08, 2015

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Neurolumen LLC
Location: Oklahoma City, Oklahoma, United States
FEI Number: 3010144038
Product Type: Devices
Issue Date: May 08, 2015
Country: United States

Inspection History, 2013 to 2025

NAI1

VAI2

OAI1

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.

Neurolumen LLC FDA Form 483, Oklahoma City, Oklahoma, May 8, 2015