# FDA Inspection 998393 - Robert C. G. Martin, II, M.D., PhD. - January 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/robert-c-g-martin-ii-md-phd/9dc4e4cb-8306-4e37-82af-b5e2ace289d2
Source feed: FDA_Inspections

> FDA Inspection 998393 for Robert C. G. Martin, II, M.D., PhD. on January 25, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998393
- Company Name: Robert C. G. Martin, II, M.D., PhD.
- Inspection Date: 2017-01-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 701939 - 2010-12-03](https://www.keypedia.com/records/fda_inspections/robert-c-g-martin-ii-md-phd/72c88a0c-7d42-41d8-9830-f86379253267)

Company: https://www.keypedia.com/companies/robert-c-g-martin-ii-md-phd/12b3780b-c865-4d25-b194-e50cf527bfd9

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