# Serf – FDA Inspection, Sep 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/serf/f6e51287-7eab-40ed-a2c0-f2a396ce2ee6
Source feed: FDA_Inspections

> FDA inspection 1026734 of Serf, September 21, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026734
- Company Name: Serf
- Inspection Date: 2017-09-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1263519 - 2025-01-30
- [FDA Inspection 841020 - 2013-06-20](https://www.keypedia.com/records/fda_inspections/serf/a9b9ebc1-bccb-4ed9-8304-0e6790087c65)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

Company: https://www.keypedia.com/companies/serf/08264a0d-5f99-4307-a0e5-82c4e2bd7230

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7