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•United States

Aurident Inc, Fullerton, CA – FDA Inspections

Inspection records and compliance data for Aurident Inc in Fullerton, California. 4 FDA inspections on record, 1 Form 483, last inspected October 15, 2026.

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Company Profile

This profile covers Aurident Inc based in Fullerton, California, United States.

FDA Inspection History

FDA inspections
4
OAI
0
VAI
2
NAI
2
Form 483s
1
Warning letters
0

First inspected December 7, 2011. Last inspected October 15, 2026.

Most cited issue areas

  • Design and development file does not include or reference required records1 inspection
  • DMR - not or inadequately maintained1 inspection
  • Lack of or inadequate DHR procedures1 inspection

FDA inspections (4)

DateResultFDA center(s)Insp. #
October 15, 2026VAI · Compliance: Devices1341670
September 27, 2018VAIMedical Devices & Rad Health · Compliance: Devices1067019
January 29, 2013NAIMedical Devices & Rad Health · Compliance: Devices816456
December 7, 2011NAIMedical Devices & Rad Health · Postmarket Assurance: Devices761092
FDA documents

No Form 483s, Warning Letters or EIRs on record.

Related Companies (10)

Companies with similar regulatory profiles, compliance history, and operations.

Bentec Medical, Inc.
Tic, LLC
Berkley Medical Resources, Inc
Mesa Laboratories, Inc., Bozeman Manufacturing Facility
Medi Manufacturing Inc
Medron, LLC
Vitalgo Inc.
Medical Instrument Development Laboratories, Inc.
Jones Medical Instrument Co.
Orthopedic Sciences Inc
Company Information

Name

Aurident Inc

FEI Number

2023817

Address

610 S State College Blvd, Fullerton, California 92831, United States

Country

United States

ID: 498bd7dc-e80f-4ded-a3cf-4aef0103af22

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