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FDA Inspection
•Persyst Development Corp•May 19, 2017

Persyst Development Corp – FDA Inspection, May 19, 2017

Record Details

This FDA Inspection record concerns Persyst Development Corp, with an inspection on May 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Persyst Development Corp
Inspection Date
May 19, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Charles L. Larson (Company Rep)
View Company Profile

ID · 615fefac-e5a8-484e-a1c9-e9dbadd1c096

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1023508
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Persyst Development Corp

2
DateClassificationOfficeProject area
April 3, 2018Not classifiedLos Angeles District Office
October 27, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Persyst Development Corp
  • FDA Inspection 1082695 - 2018-04-03
  • FDA Inspection 751467 - 2011-10-27

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