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FDA Inspection
•MichClone Associates, Inc.•November 22, 2011

MichClone Associates, Inc. – FDA Inspection, Nov 22, 2011

Record Details

This FDA Inspection record concerns MichClone Associates, Inc., with an inspection on November 22, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
MichClone Associates, Inc.
Inspection Date
November 22, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 7c1330bb-e645-4faa-9653-32d0386db304

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
753208
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of MichClone Associates, Inc.

5
DateClassificationOfficeProject area
September 4, 2025NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 17, 2021VAICenter for Devices and Radiological HealthCompliance: Devices
March 9, 2017NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 3, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 2, 2010VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for MichClone Associates, Inc.
  • FDA Inspection 1281306 - 2025-09-04
  • FDA Inspection 1158990 - 2021-12-17
  • FDA Inspection 1003228 - 2017-03-09
  • FDA Inspection 882137 - 2014-06-03
  • FDA Inspection 670119 - 2010-07-02

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