FDA Inspection
SerfSerf – FDA Inspection, Sep 21, 2017
Record Details
This FDA Inspection record concerns Serf, with an inspection on September 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f6e51287-7eab-40ed-a2c0-f2a396ce2ee6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1026734
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Serf
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 30, 2025 | Not classified | Office of Inspections and Investigations | |
| June 20, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Serf
- FDA Inspection 1263519 - 2025-01-30
- FDA Inspection 841020 - 2013-06-20
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