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FDA Inspection
•Sachar, Ravish Md•May 30, 2018

Sachar, Ravish Md – FDA Inspection, May 30, 2018

Record Details

This FDA Inspection record concerns Sachar, Ravish Md, with an inspection on May 30, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Sachar, Ravish Md
Inspection Date
May 30, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • William P Tonkins (Issuing Officer)
View Company Profile

ID · ab3554ce-ac68-4758-b8aa-faea59e30c8e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1053634
FDA center
Medical Devices & Rad Health
Project area
Project Evaluation: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Sachar, Ravish Md

2
DateClassificationOfficeProject area
July 10, 2014NAICenter for Devices and Radiological HealthBioresearch Monitoring
October 15, 2010NAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Sachar, Ravish Md
  • FDA Inspection 887047 - 2014-07-10
  • FDA Inspection 696006 - 2010-10-15

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