FDA Inspection
Robert Lehmann, Dr/Clin InvRobert Lehmann, Dr/Clin Inv – FDA Inspection, Oct 31, 2019
Record Details
This FDA Inspection record concerns Robert Lehmann, Dr/Clin Inv, with an inspection on October 31, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Robert Lehmann, Dr/Clin Inv
- Inspection Date
- October 31, 2019
- Product Type
- Devices
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ID · d691fae4-8990-4d92-b61c-ba4d33ddc1f7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1108510
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of Robert Lehmann, Dr/Clin Inv
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 5, 2016 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 21, 2010 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Robert Lehmann, Dr/Clin Inv
- FDA Inspection 971438 - 2016-05-05
- FDA Inspection 685907 - 2010-10-21
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