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FDA Inspection
•MICROVENTION INC.•September 25, 2015

MICROVENTION INC. – FDA Inspection, Sep 25, 2015

Record Details

This FDA Inspection record concerns MICROVENTION INC., with an inspection on September 25, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
MICROVENTION INC.
Inspection Date
September 25, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 6819729d-39be-4b86-a4a6-aca1c2764a34

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
943775
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of MICROVENTION INC.

5
DateClassificationOfficeProject area
May 4, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
June 22, 2021NAICenter for Devices and Radiological HealthCompliance: Devices
January 17, 2019NAICenter for Devices and Radiological HealthBioresearch Monitoring
November 29, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
December 13, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for MICROVENTION INC.
  • FDA Inspection 1205080 - 2023-05-04
  • FDA Inspection 1155400 - 2021-06-22
  • FDA Inspection 1077480 - 2019-01-17
  • FDA Inspection 1074141 - 2018-11-29
  • FDA Inspection 757144 - 2011-12-13

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