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FDA Inspection
•Crown Delta Corp•April 4, 2017

Crown Delta Corp – FDA Inspection, Apr 4, 2017

Record Details

This FDA Inspection record concerns Crown Delta Corp, with an inspection on April 4, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Crown Delta Corp
Inspection Date
April 4, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Kwong P. Lee (Company Rep)
View Company Profile

ID · d9fb4bfb-4450-4c20-bf44-70219b901822

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1014734
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.72(a)Equipment control activity documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Crown Delta Corp

3
DateClassificationOfficeProject area
October 31, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
March 4, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
November 23, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Crown Delta Corp
  • FDA Inspection 1192125 - 2022-10-31
  • FDA Inspection 866895 - 2014-03-04
  • FDA Inspection 699915 - 2010-11-23

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