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FDA Inspection
•Adler MicroMed, Inc.•April 23, 2019

Adler MicroMed, Inc. – FDA Inspection, Apr 23, 2019

Record Details

This FDA Inspection record concerns Adler MicroMed, Inc., with an inspection on April 23, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Adler MicroMed, Inc.
Inspection Date
April 23, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • James A. Lane (FDA Associated Person)
View Company Profile

ID · d4465f0c-3ad6-426d-97ea-8f419fc3bed8

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1089915
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Adler MicroMed, Inc.

3
DateClassificationOfficeProject area
February 12, 2026VAILos Angeles District OfficeCompliance: Medical Devices
August 24, 2023NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
May 17, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Adler MicroMed, Inc.
  • FDA Inspection 1302886 - 2026-02-12
  • FDA Inspection 1218559 - 2023-08-24
  • FDA Inspection 974410 - 2016-05-17

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