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FDA Inspection
•Lymol Medical Corporation•February 12, 2020

Lymol Medical Corporation – FDA Inspection, Feb 12, 2020

Record Details

This FDA Inspection record concerns Lymol Medical Corporation, with an inspection on February 12, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company
Lymol Medical Corporation
Inspection Date
February 12, 2020
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 933ff1ee-2777-4d54-9b0c-e5dc8212dcb1

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1117620
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Enforcement
Warning Letter

Other FDA inspections of Lymol Medical Corporation

5
DateClassificationOfficeProject area
July 29, 2021OAICenter for Devices and Radiological HealthCompliance: Devices
June 24, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 15, 2011VAICenter for Drug Evaluation and ResearchPostmarket Surv. and Epidemiology
September 14, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
July 9, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Lymol Medical Corporation
  • FDA Inspection 1147369 - 2021-07-29
  • FDA Inspection 976447 - 2016-06-24
  • FDA Inspection 759069 - 2011-12-15
  • FDA Inspection 680212 - 2010-09-14
  • FDA Inspection 596000 - 2009-07-09

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