# FDA Inspection 998803 - Pamela M. Otto, M.D. - November 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/pamela-m-otto-md/3029179e-e4fb-4383-8aaf-2d405dbca60c
Source feed: FDA_Inspections

> FDA Inspection 998803 for Pamela M. Otto, M.D. on November 18, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998803
- Company Name: Pamela M. Otto, M.D.
- Inspection Date: 2016-11-18
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1170698 - 2022-05-18](https://www.keypedia.com/records/fda_inspections/pamela-m-otto-md/657741ae-ed9c-4ce8-ad44-de1c8f3c3fc9)

Company: https://www.keypedia.com/companies/pamela-m-otto-md/42755098-5c2f-44cd-9483-782f343fd94c

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