Verity Medical Ltd. – FDA Inspection, Nov 8, 2017

Record Details

This FDA Inspection record concerns Verity Medical Ltd., with an inspection on November 8, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Verity Medical Ltd.
Inspection Date: November 8, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Melanie W. Pishnery

View Company Profile

ID · 46152ad5-657c-4ef9-8ad9-ff2685ec51a1

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1030936
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices
Outcome: Form 483 issued

FDA Citations

21 CFR 820.90(b)(2)Product rework documentation, DHR {see also 820.184}

Full citation text and observation details available on the Dashboard.

Discuss this record with AI

KeyPedia

ChatGPT

Claude

Perplexity

Grok

Copilot

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.

Explore Verity Medical Ltd.

FDA Inspection

Verity Medical Ltd.November 8, 2017