FDA Inspection
Renovo Life LLCRenovo Life LLC – FDA Inspection, Jan 26, 2018
Record Details
This FDA Inspection record concerns Renovo Life LLC, with an inspection on January 26, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 2973a70a-70d6-4fc6-b643-9b69f28ad90f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1038739
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.120(b)DHR documentation of label release {see also 820.184}
- 21 CFR 820.184DHR content
- 21 CFR 820.90(a)Nonconforming product control
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