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FDA Inspection
•Valplast International Corp•October 19, 2012

Valplast International Corp – FDA Inspection, Oct 19, 2012

Record Details

This FDA Inspection record concerns Valplast International Corp, with an inspection on October 19, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
Valplast International Corp
Inspection Date
October 19, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · b36f0afc-04f8-4a16-9278-0f83f1fb785b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
806824
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 820.80(b)Incoming acceptance records, documentation
  2. 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Valplast International Corp

4
DateClassificationOfficeProject area
January 25, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
February 25, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
February 1, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 18, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Valplast International Corp
  • FDA Inspection 1039419 - 2018-01-25
  • FDA Inspection 915935 - 2015-02-25
  • FDA Inspection 708721 - 2011-02-01
  • FDA Inspection 570706 - 2009-03-18

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