FDA Inspection
Max Mobility LLCFDA Inspection 923083 - Max Mobility LLC - April 24, 2015
Record Details
This FDA Inspection record concerns Max Mobility LLC, with an inspection on April 24, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Max Mobility LLC
- Inspection Date
- April 24, 2015
- Product Type
- Devices
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ID · 8d76efa9-300c-4a95-b0d5-574a21b89331
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 923083
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Max Mobility LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 16, 2026 | Not classified | New Orleans District Office | Compliance: Devices |
| December 7, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 7, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 27, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Max Mobility LLC
- FDA Inspection 1312046 - 2026-04-16
- FDA Inspection 1224396 - 2023-12-07
- FDA Inspection 1030858 - 2017-11-07
- FDA Inspection 871149 - 2014-03-27
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