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FDA Inspection
•Charles Klodell, MD•November 3, 2016

Charles Klodell, MD – FDA Inspection, Nov 3, 2016

Record Details

This FDA Inspection record concerns Charles Klodell, MD, with an inspection on November 3, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Charles Klodell, MD
Inspection Date
November 3, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Leon L. Crawley (Investigator)
  • Traci M. Armand (Company Rep)
View Company Profile

ID · bb3957df-d82c-4aa9-ac25-bda041522228

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
991988
FDA center
Medical Devices & Rad Health
Project area
Project Evaluation: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations

Full citation text and observation details available on the Dashboard.

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