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FDA Inspection
•LD Technology, LLC•June 29, 2010

LD Technology, LLC – FDA Inspection, Jun 29, 2010

Record Details

This FDA Inspection record concerns LD Technology, LLC, with an inspection on June 29, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
LD Technology, LLC
Inspection Date
June 29, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 764e6e00-e06b-4d96-bb40-900366c9bd6a

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
670694
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

4
  1. 21 CFR 820.30(c)Design input - documentation
  2. 21 CFR 820.30(g)Design validation - user needs and intended uses
  3. 21 CFR 820.22Quality Audits - defined intervals
  4. 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements

Full citation text and observation details available on the Dashboard.

Other FDA inspections of LD Technology, LLC

5
DateClassificationOfficeProject area
November 14, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
November 9, 2022NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 13, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
May 5, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
October 27, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for LD Technology, LLC
  • FDA Inspection 1255679 - 2024-11-14
  • FDA Inspection 1190293 - 2022-11-09
  • FDA Inspection 1112610 - 2019-12-13
  • FDA Inspection 924934 - 2015-05-05
  • FDA Inspection 754378 - 2011-10-27

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