# FDA Inspection 830698 - Robert Cywes, M.D. - May 01, 2013

Source: https://www.keypedia.com/records/fda_inspections/robert-cywes-md/68a8c3fb-1ef8-4774-a724-6c33a87062f8
Source feed: FDA_Inspections

> FDA Inspection 830698 for Robert Cywes, M.D. on May 01, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830698
- Company Name: Robert Cywes, M.D.
- Inspection Date: 2013-05-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 712894 - 2011-03-09](https://www.keypedia.com/records/fda_inspections/robert-cywes-md/39ff14a2-ff9b-408f-8477-bbe5d5f4efab)

Company: https://www.keypedia.com/companies/robert-cywes-md/44de6722-05cf-4b92-992f-929a67c05cdf

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