# FDA Inspection 1026734 - Serf - September 21, 2017

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

> FDA Inspection 1026734 for Serf on September 21, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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