# FDA Inspection 1083561 - Scantibodies Laboratory, Inc. - March 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/scantibodies-laboratory-inc/1dc4bc26-b2f1-414b-b94c-4cf7e0bd50e4
Source feed: FDA_Inspections

> FDA Inspection 1083561 for Scantibodies Laboratory, Inc. on March 14, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1083561
- Company Name: Scantibodies Laboratory, Inc.
- Inspection Date: 2019-03-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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