# Scantibodies Laboratory, Inc. – FDA Inspection, Mar 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/scantibodies-laboratory-inc/503380fa-fe8f-4ae9-9e72-a2765ca6c1ab
Source feed: FDA_Inspections

> FDA inspection 1083561 of Scantibodies Laboratory, Inc., March 14, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1083561
- Company Name: Scantibodies Laboratory, Inc.
- Inspection Date: 2019-03-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1325322 - 2026-07-02](https://www.keypedia.com/records/fda_inspections/scantibodies-laboratory-inc/ccc4141a-af7f-4f2d-8073-23cc5b7ad2dd)
- [FDA Inspection 881586 - 2014-06-16](https://www.keypedia.com/records/fda_inspections/scantibodies-laboratory-inc/09113afa-03a5-4481-b686-736e8de6f969)
- [FDA Inspection 829760 - 2013-05-24](https://www.keypedia.com/records/fda_inspections/scantibodies-laboratory-inc/478d5d42-6adb-4a43-8377-376990daaa07)
- FDA Inspection 760535 - 2011-12-19
- [FDA Inspection 754602 - 2011-11-21](https://www.keypedia.com/records/fda_inspections/scantibodies-laboratory-inc/c0d73313-4259-466e-a0e7-5befcb7dc97f)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.keypedia.com/companies/scantibodies-laboratory-inc/87cffccc-0129-4ca1-b942-54c86ecde06f

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7