# Robert Lehmann, Dr/Clin Inv – FDA Inspection, Oct 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/robert-lehmann-drclin-inv/d691fae4-8990-4d92-b61c-ba4d33ddc1f7
Source feed: FDA_Inspections

> FDA inspection 1108510 of Robert Lehmann, Dr/Clin Inv, October 31, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1108510
- Company Name: Robert Lehmann, Dr/Clin Inv
- Inspection Date: 2019-10-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 971438 - 2016-05-05
- FDA Inspection 685907 - 2010-10-21

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