OmniLife Science

Form 483

Raynham, Massachusetts, United StatesFEI 3008342029Issued December 06, 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 3008342029.

Observations3

Issue DateDecember 06, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: OmniLife Science
Location: Raynham, Massachusetts, United States
FEI Number: 3008342029
Product Type: Devices
Issue Date: December 06, 2012
Country: United States

Inspection History, 2011 to 2022

NAI2

VAI2

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.

OmniLife Science FDA Form 483, Raynham, Massachusetts, December 6, 2012