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FDA Inspection
•Lloyd Industries Inc.•November 23, 2010

Lloyd Industries Inc. – FDA Inspection, Nov 23, 2010

Record Details

This FDA Inspection record concerns Lloyd Industries Inc., with an inspection on November 23, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Lloyd Industries Inc.
Inspection Date
November 23, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c185e4c4-106e-4492-b7d7-d09bc008bd60

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
698848
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

3
  1. 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
  2. 21 CFR 820.75(a)Documentation
  3. 21 CFR 820.30(e)Design review - documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Lloyd Industries Inc.

4
DateClassificationOfficeProject area
April 3, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
September 12, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
January 29, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
August 1, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Lloyd Industries Inc.
  • FDA Inspection 1229379 - 2024-04-03
  • FDA Inspection 1103430 - 2019-09-12
  • FDA Inspection 914122 - 2015-01-29
  • FDA Inspection 737821 - 2011-08-01

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