# FDA Inspection 685907 - Robert Lehmann, Dr/Clin Inv - October 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/robert-lehmann-drclin-inv/c4b62ef0-d48e-4ba3-b384-9eadadb1aed3
Source feed: FDA_Inspections

> FDA Inspection 685907 for Robert Lehmann, Dr/Clin Inv on October 21, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 685907
- Company Name: Robert Lehmann, Dr/Clin Inv
- Inspection Date: 2010-10-21
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1108510 - 2019-10-31](https://www.keypedia.com/records/fda_inspections/robert-lehmann-drclin-inv/d691fae4-8990-4d92-b61c-ba4d33ddc1f7)
- [FDA Inspection 971438 - 2016-05-05](https://www.keypedia.com/records/fda_inspections/robert-lehmann-drclin-inv/faf0f207-bf67-41bc-9cfa-09d9aba6b693)

Company: https://www.keypedia.com/companies/robert-lehmann-drclin-inv/1df5ffff-1a52-44c9-8fa9-235e2c53fe79

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