# FDA Inspection 1117355 - Richard D. Guyer, MD - February 10, 2020

Source: https://www.globalkeysolutions.net/records/fda_inspections/richard-d-guyer-md/5a0b8ad7-4d57-4a32-afde-69d84cac2560
Source feed: FDA_Inspections

> FDA Inspection 1117355 for Richard D. Guyer, MD on February 10, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1117355
- Company Name: Richard D. Guyer, MD
- Inspection Date: 2020-02-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 576507 - 2009-04-07](https://www.globalkeysolutions.net/records/fda_inspections/richard-d-guyer-md/4c38ea90-7007-4cdc-a330-25f460352eec)

Company: https://www.globalkeysolutions.net/companies/richard-d-guyer-md/0b1e8b77-c09a-4144-8147-39ed4c0bc711

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