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FDA Inspection
•Sonoco Plastics B.V•August 22, 2019

Sonoco Plastics B.V – FDA Inspection, Aug 22, 2019

Record Details

This FDA Inspection record concerns Sonoco Plastics B.V, with an inspection on August 22, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Sonoco Plastics B.V
Inspection Date
August 22, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Shaquenta Y. Perkins (Issuing Officer)
View Company Profile

ID · 3a740e64-a4e7-4f56-a9a4-6830c39b163d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1101658
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
  2. 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Sonoco Plastics B.V

1
DateClassificationOfficeProject area
June 30, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Sonoco Plastics B.V
  • FDA Inspection 979543 - 2016-06-30

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