KMI IMI Group dba Innovative Med Inc.

Form 483

Irvine, California, United StatesFEI 3004112621Issued August 05, 2010

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 3004112621.

Observations2

Issue DateAugust 05, 2010

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: KMI IMI Group dba Innovative Med Inc.
Location: Irvine, California, United States
FEI Number: 3004112621
Product Type: Devices
Issue Date: August 05, 2010
Country: United States

Inspection History, 2010 to 2025

NAI3

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.

KMI IMI Group dba Innovative Med Inc. FDA Form 483, Irvine, California, August 5, 2010