FDA Inspection
SerfSerf – FDA Inspection, Jun 20, 2013
Record Details
This FDA Inspection record concerns Serf, with an inspection on June 20, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Serf
- Inspection Date
- June 20, 2013
- Product Type
- Devices
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ID · a9b9ebc1-bccb-4ed9-8304-0e6790087c65
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 841020
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.30(c)Design input - documentation
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Serf
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 30, 2025 | Not classified | Office of Inspections and Investigations | |
| September 21, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Serf
- FDA Inspection 1263519 - 2025-01-30
- FDA Inspection 1026734 - 2017-09-21
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