Medefil Incorporated

Form 483

Glendale Heights, Illinois, United StatesFEI 3001677091Issued September 15, 2014

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 3001677091.

Observations5

Issue DateSeptember 15, 2014

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Medefil Incorporated
Location: Glendale Heights, Illinois, United States
FEI Number: 3001677091
Product Type: Devices
Issue Date: September 15, 2014
Country: United States

Inspection History, 2010 to 2025

NAI2

VAI6

OAI2

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.

Medefil Incorporated FDA Form 483, Glendale Heights, Illinois, September 15, 2014