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FDA Inspection
•Resilience US, Inc.•May 28, 2009

Resilience US, Inc. – FDA Inspection, May 28, 2009

Record Details

This FDA Inspection record concerns Resilience US, Inc., with an inspection on May 28, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Resilience US, Inc.
Inspection Date
May 28, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 7b596ad0-4510-42d1-905d-68d66c75d54a

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
595314
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Resilience US, Inc.

6
DateClassificationOfficeProject area
August 21, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 14, 2017NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
August 11, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 25, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 13, 2009OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Resilience US, Inc.
  • FDA Inspection 1102300 - 2019-08-21
  • FDA Inspection 1028333 - 2017-09-14
  • FDA Inspection 1021959 - 2017-08-11
  • FDA Inspection 897817 - 2014-09-25
  • FDA Inspection 625796 - 2009-11-13

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