Scantibodies Laboratory, Inc.

Form 483

Santee, California, United StatesFEI 2020808Issued November 21, 2011

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 2020808.

Observations4

Issue DateNovember 21, 2011

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Scantibodies Laboratory, Inc.
Location: Santee, California, United States
FEI Number: 2020808
Product Type: Devices
Issue Date: November 21, 2011
Country: United States

Inspection History, 2011 to 2019

NAI1

VAI3

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.

Scantibodies Laboratory, Inc. FDA Form 483, Santee, California, November 21, 2011