FDA inspection

Scantibodies Laboratory, Inc.: FDA inspection ending Nov 21, 2011

FDA inspection 754602 · Voluntary Action Indicated (VAI) · Santee, CA

Key facts

Inspection ID 754602
Firm Scantibodies Laboratory, Inc.
FEI number 2020808
Address 9336 Abraham Way
City Santee
State CA
ZIP 92071
Country United States
Fiscal year 2012
Inspection end date Nov 21, 2011
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

Browse all FDA inspections