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FDA Inspection
•Medical Action Industries, Inc. 306•April 11, 2017

Medical Action Industries, Inc. 306 – FDA Inspection, Apr 11, 2017

Record Details

This FDA Inspection record concerns Medical Action Industries, Inc. 306, with an inspection on April 11, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Medical Action Industries, Inc. 306
Inspection Date
April 11, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Claudette D. Brooks (FDA Associated Person)
View Company Profile

ID · 9daa368f-ab4f-4359-bb29-8a49dc12d2e4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1028761
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 820.80(e)Documentation
  2. 21 CFR 820.70(b)Production and Process Change Procedures, lack of or Inad.
  3. 21 CFR 820.100(a)Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Medical Action Industries, Inc. 306

3
DateClassificationOfficeProject area
August 15, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
October 30, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
March 31, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Medical Action Industries, Inc. 306
  • FDA Inspection 1218286 - 2023-08-15
  • FDA Inspection 808024 - 2012-10-30
  • FDA Inspection 579411 - 2009-03-31

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