FDA Inspection
Lauryssen, CarlLauryssen, Carl – FDA Inspection, May 26, 2010
Record Details
This FDA Inspection record concerns Lauryssen, Carl, with an inspection on May 26, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lauryssen, Carl
- Inspection Date
- May 26, 2010
- Product Type
- Devices
View Company Profile
ID · 98f47385-fce6-4d98-80d3-03b8b0c8c732
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 663710
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.100Investigator lack of informed consent
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Lauryssen, Carl
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 17, 2021 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Lauryssen, Carl
- FDA Inspection 1154953 - 2021-09-17
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.