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FDA Inspection
•Cadwell Industries Inc•April 30, 2013

Cadwell Industries Inc – FDA Inspection, Apr 30, 2013

Record Details

This FDA Inspection record concerns Cadwell Industries Inc, with an inspection on April 30, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Cadwell Industries Inc
Inspection Date
April 30, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 7cebe67d-ba11-46ad-a973-50c0237b7530

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
829514
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

3
  1. 21 CFR 803.50(a)(1)Report of Death or Serious Injury
  2. 21 CFR 820.100(a)Lack of or inadequate procedures
  3. 21 CFR 820.184Lack of or inadequate DHR procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Cadwell Industries Inc

1
DateClassificationOfficeProject area
August 16, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Cadwell Industries Inc
  • FDA Inspection 1023280 - 2017-08-16

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