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FDA Inspection
•Multi-Med, Inc.•September 11, 2009

Multi-Med, Inc. – FDA Inspection, Sep 11, 2009

Record Details

This FDA Inspection record concerns Multi-Med, Inc., with an inspection on September 11, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Multi-Med, Inc.
Inspection Date
September 11, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 1dec0609-1176-49cd-87a6-acba767354a4

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
613087
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Multi-Med, Inc.

6
DateClassificationOfficeProject area
September 19, 2024NAINew England District OfficePostmarket Assurance: Medical Devices
August 16, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
June 18, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
May 11, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
July 8, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
View all 6 other inspections on the company page
Other documents for Multi-Med, Inc.
  • FDA Inspection 1229145 - 2024-09-19
  • FDA Inspection 1022895 - 2017-08-16
  • FDA Inspection 883593 - 2014-06-18
  • FDA Inspection 781212 - 2012-05-11
  • FDA Inspection 667190 - 2010-07-08

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