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FDA Inspection
•Stellartech Research Corporation•December 12, 2018

Stellartech Research Corporation – FDA Inspection, Dec 12, 2018

Record Details

This FDA Inspection record concerns Stellartech Research Corporation, with an inspection on December 12, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Stellartech Research Corporation
Inspection Date
December 12, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Daniel J. Lahar (FDA Associated Person)
View Company Profile

ID · e977c5b4-dbd1-4313-894a-5aaef63e2179

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1076850
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

Other FDA inspections of Stellartech Research Corporation

7
DateClassificationOfficeProject area
April 23, 2025NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 29, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 20, 2015NAICenter for Devices and Radiological HealthBioresearch Monitoring
August 14, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 19, 2013VAICenter for Devices and Radiological HealthBioresearch Monitoring
View all 7 other inspections on the company page
Other documents for Stellartech Research Corporation
  • FDA Inspection 1268787 - 2025-04-23
  • FDA Inspection 1202527 - 2023-03-29
  • FDA Inspection 939415 - 2015-08-20
  • FDA Inspection 892384 - 2014-08-14
  • FDA Inspection 818944 - 2013-02-19

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