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FDA Inspection
•Epimed International, Inc.•December 12, 2018

Epimed International, Inc. – FDA Inspection, Dec 12, 2018

Record Details

This FDA Inspection record concerns Epimed International, Inc., with an inspection on December 12, 2018, issued by the New York District Office, covering medical devices & rad health.

Company
Epimed International, Inc.
Inspection Date
December 12, 2018
Product Type
Medical Devices & Rad Health
Office
New York District Office
View Company Profile

ID · afaf2aaf-17da-4489-adc3-ff8fc7932d87

Inspection Facts

Inspection number
1094942
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Epimed International, Inc.

5
DateClassificationOfficeProject area
July 12, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
November 6, 2013NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 26, 2013VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 17, 2012OAICenter for Devices and Radiological HealthCompliance: Devices
April 13, 2010VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Epimed International, Inc.
  • FDA Inspection 977666 - 2016-07-12
  • FDA Inspection 855890 - 2013-11-06
  • FDA Inspection 823868 - 2013-03-26
  • FDA Inspection 781198 - 2012-05-17
  • FDA Inspection 657836 - 2010-04-13

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