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FDA Inspection
•Innovative Med Inc.•August 5, 2010

Innovative Med Inc. – FDA Inspection, Aug 5, 2010

Record Details

This FDA Inspection record concerns Innovative Med Inc., with an inspection on August 5, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Innovative Med Inc.
Inspection Date
August 5, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 49f69f59-acb0-459c-91ac-b512d3366546

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
675156
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 820.181DMR - not or inadequately maintained
  2. 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Innovative Med Inc.

5
DateClassificationOfficeProject area
April 15, 2025NAILos Angeles District OfficePostmarket Assurance: Medical Devices
March 8, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
December 17, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
October 9, 2012OAICenter for Devices and Radiological HealthCompliance: Devices
August 17, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Innovative Med Inc.
  • FDA Inspection 1266957 - 2025-04-15
  • FDA Inspection 1044034 - 2018-03-08
  • FDA Inspection 859340 - 2013-12-17
  • FDA Inspection 803087 - 2012-10-09
  • FDA Inspection 740161 - 2011-08-17

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