FDA Inspection
Medlogix, LLCMedlogix, LLC – FDA Inspection, May 14, 2019
Record Details
This FDA Inspection record concerns Medlogix, LLC, with an inspection on May 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 1bf1596d-0fc8-49d8-95f1-a298a06911dc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1092546
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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