FDA Inspection
Perfuze LTDPerfuze LTD – FDA Inspection, May 22, 2024
Record Details
This FDA Inspection record concerns Perfuze LTD, with an inspection on May 22, 2024, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · fde0c7a3-8ebb-4fe0-ad26-47ffcc84eeb5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1239139
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.250(a)Statistical techniques - Lack of or inadequate procedures
- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
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.