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FDA Inspection
•Ultralite Enterprises Inc•June 29, 2022

Ultralite Enterprises Inc – FDA Inspection, Jun 29, 2022

Record Details

This FDA Inspection record concerns Ultralite Enterprises Inc, with an inspection on June 29, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company
Ultralite Enterprises Inc
Inspection Date
June 29, 2022
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · e745c4a7-2b83-42d6-9f98-a3134c64e87e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1175673
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Ultralite Enterprises Inc

4
DateClassificationOfficeProject area
May 12, 2016NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 1, 2012NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
April 18, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
January 29, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Ultralite Enterprises Inc
  • FDA Inspection 971960 - 2016-05-12
  • FDA Inspection 805763 - 2012-11-01
  • FDA Inspection 720264 - 2011-04-18
  • FDA Inspection 570532 - 2009-01-29

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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