# Robert C. G. Martin, II, M.D., PhD. – FDA Inspection, Jan 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/robert-c-g-martin-ii-md-phd/dc006ed9-d492-43e6-a0fb-20f220b05da7
Source feed: FDA_Inspections

> FDA inspection 998393 of Robert C. G. Martin, II, M.D., PhD., January 25, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 701939 - 2010-12-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/craig-t-rybus/246aad79-6370-42e2-af6e-c0079c1bcbc6)

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
