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FDA Inspection
•Max Mobility LLC•April 16, 2026

FDA Inspection 1312046 - Max Mobility LLC - April 16, 2026

Record Details

This FDA Inspection record concerns Max Mobility LLC, with an inspection on April 16, 2026, issued by the New Orleans District Office, covering medical devices & rad health.

Company
Max Mobility LLC
Inspection Date
April 16, 2026
Product Type
Medical Devices & Rad Health
Office
New Orleans District Office
Person
  • Jamie P. Webb (Issuing Officer)
View Company Profile

ID · e42192c4-b665-4e20-aa41-149bea1b825f

Inspection Facts

Inspection number
1312046
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. ISO 13485:2016 Clause 7.3.9Procedures to control design and development changes not documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Max Mobility LLC

4
DateClassificationOfficeProject area
December 7, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
November 7, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
April 24, 2015VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 27, 2014OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Max Mobility LLC
  • FDA Inspection 1224396 - 2023-12-07
  • FDA Inspection 1030858 - 2017-11-07
  • FDA Inspection 923083 - 2015-04-24
  • FDA Inspection 871149 - 2014-03-27

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