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FDA Inspection
•Saint-Gobain Perofrmance Plastics, Inc.•July 28, 2023

Saint-Gobain Perofrmance Plastics, Inc. – FDA Inspection, Jul 28, 2023

Record Details

This FDA Inspection record concerns Saint-Gobain Perofrmance Plastics, Inc., with an inspection on July 28, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Saint-Gobain Perofrmance Plastics, Inc.
Inspection Date
July 28, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Tyler R. Courtney (Company Rep)
View Company Profile

ID · 720ee325-8854-4f65-ab26-427f624f9bf9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1211625
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.100(a)Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Saint-Gobain Perofrmance Plastics, Inc.

1
DateClassificationOfficeProject area
April 7, 2026NAIPostmarket Assurance: Devices
Other documents for Saint-Gobain Perofrmance Plastics, Inc.
  • FDA Inspection 1312350 - 2026-04-07

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