FDA Inspection
Gobiquity, IncGobiquity, Inc – FDA Inspection, Aug 17, 2018
Record Details
This FDA Inspection record concerns Gobiquity, Inc, with an inspection on August 17, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b3465be5-9c72-41de-9d3e-f36bce184b0e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1062903
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Gobiquity, Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2026 | VAI | New Orleans District Office | Compliance: Medical Devices |
| June 15, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 17, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
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