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•United States

DIO USA, Los Angeles, CA – FDA Inspections

Inspection records and compliance data for DIO USA in Los Angeles, California. 2 FDA inspections on record, last inspected May 12, 2010.

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Company Profile

This profile covers DIO USA based in Los Angeles, California, United States.

FDA Inspection History

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

First inspected November 16, 2009. Last inspected May 12, 2010.

Most cited issue areas

  • Distributor responsibilities for complaint records2 inspections
  • Lack of Written MDR Procedures1 inspection

FDA inspections (2)

DateResultFDA center(s)Insp. #
May 12, 2010VAIMedical Devices & Rad Health · Compliance: Devices661058
November 16, 2009VAIMedical Devices & Rad Health · Compliance: Devices627607
FDA documents

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

Related Companies (10)

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

Endologix, Inc.
Nexus Dx, Inc
Mahmud, Ehtisham MD
Boston Scientific Corporation
Sanarus Technologies Inc.
Rox Medical Inc
GD Designs, Inc.
Reciprocal Labs Corporation
Cortechs Labs, Inc.
Rubin, Mark, G., MD
Company Information

Name

DIO USA

FEI Number

3006400105

Address

3540 Wilshire Blvd Ste 1104, Los Angeles, California 90010, United States

Country

United States

ID: 00671082-a024-47e9-b139-1857c67e07ab

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