FDA Inspection
RIMOS SRLRIMOS SRL – FDA Inspection, Mar 29, 2012
Record Details
This FDA Inspection record concerns RIMOS SRL, with an inspection on March 29, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- RIMOS SRL
- Inspection Date
- March 29, 2012
- Product Type
- Devices
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ID · 952cbaa0-1f09-43a3-8182-d63d946d218e
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 778367
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
8- 21 CFR 820.80(b)Incoming acceptance records, documentation
- 21 CFR 820.70(f)Buildings
- 21 CFR 820.72(b)Calibration procedures - content
- 21 CFR 820.120(d)Mixups
- 21 CFR 820.25(a)Personnel
- 21 CFR 820.75(a)Documentation
- 21 CFR 820.22Quality Audits - defined intervals
- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
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Other FDA inspections of RIMOS SRL
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 23, 2026 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
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