# FDA Inspection 983479 - Jane L. Rohlf, MD - July 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/jane-l-rohlf-md/339ff2c0-ddb6-4ba2-a859-609714626f04
Source feed: FDA_Inspections

> FDA Inspection 983479 for Jane L. Rohlf, MD on July 19, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 983479
- Company Name: Jane L. Rohlf, MD
- Inspection Date: 2016-07-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1167083 - 2022-03-31](https://www.keypedia.com/records/fda_inspections/jane-l-rohlf-md/2f3a86d4-25c2-4260-9f23-9413abfb9b1a)
- [FDA Inspection 1054870 - 2018-06-01](https://www.keypedia.com/records/fda_inspections/jane-l-rohlf-md/d5447537-2d31-47e8-8d5d-d14ab4f7cdb3)

Company: https://www.keypedia.com/companies/jane-l-rohlf-md/50dba018-a2d4-447a-8743-df5b438e8a30

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