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FDA Inspection
•Neurodynamics, Inc.•February 28, 2024

Neurodynamics, Inc. – FDA Inspection, Feb 28, 2024

Record Details

This FDA Inspection record concerns Neurodynamics, Inc., with an inspection on February 28, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Neurodynamics, Inc.
Inspection Date
February 28, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Kwong P. Lee (Company Rep)
View Company Profile

ID · a71b9e0c-4e09-497d-896b-a127ea2c3667

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1231517
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

1
  1. 21 CFR 803.17Lack of Written MDR Procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Neurodynamics, Inc.

2
DateClassificationOfficeProject area
July 21, 2021NAICenter for Devices and Radiological HealthCompliance: Devices
October 4, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Neurodynamics, Inc.
  • FDA Inspection 1146691 - 2021-07-21
  • FDA Inspection 1027756 - 2017-10-04

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