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FDA Inspection
•Quadric BioMed, LLC•December 16, 2024

FDA Inspection 1256854 - Quadric BioMed, LLC - December 16, 2024

Record Details

This FDA Inspection record concerns Quadric BioMed, LLC, with an inspection on December 16, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Quadric BioMed, LLC
Inspection Date
December 16, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Matthew M. Vernon (Company Rep)
View Company Profile

ID · 2a765e90-b352-42f1-9964-d3edc8c8dc49

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1256854
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued, view the record

FDA Citations

4
  1. 21 CFR 820.20(c)Management review - Lack of or inadequate procedures
  2. 21 CFR 820.22Quality audits - Lack of or inadequate procedures
  3. 21 CFR 820.25(b)Training - Lack of or inadequate procedures
  4. 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures

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