FDA Inspection
Jason M. Perrin, MDJason M. Perrin, MD – FDA Inspection, Mar 10, 2017
Record Details
This FDA Inspection record concerns Jason M. Perrin, MD, with an inspection on March 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Cara M. Minelli (Issuing Officer)
View Company Profile
ID · e8064183-8821-4997-9f1b-55ffd841c31b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1005490
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.100Investigator lack of control of investigational devices
- 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(3)Investigator's subject records inadequate
Full citation text and observation details available on the Dashboard.
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.