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FDA Inspection
•Freeman Enterprise LLC•March 7, 2019

Freeman Enterprise LLC – FDA Inspection, Mar 7, 2019

Record Details

This FDA Inspection record concerns Freeman Enterprise LLC, with an inspection on March 7, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Freeman Enterprise LLC
Inspection Date
March 7, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Suyang Qin (FDA Associated Person)
View Company Profile

ID · 9b8c1922-d951-4916-a00d-fea7f578f1a5

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1081836
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.198(a)Lack of or inadequate complaint procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Freeman Enterprise LLC

4
DateClassificationOfficeProject area
December 16, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
March 29, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 23, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
September 4, 2009NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Freeman Enterprise LLC
  • FDA Inspection 907129 - 2014-12-16
  • FDA Inspection 716628 - 2011-03-29
  • FDA Inspection 668234 - 2010-06-23
  • FDA Inspection 611065 - 2009-09-04

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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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