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FDA Inspection
•QuVa Pharma, Inc.•March 14, 2019

QuVa Pharma, Inc. – FDA Inspection, Mar 14, 2019

Record Details

This FDA Inspection record concerns QuVa Pharma, Inc., with an inspection on March 14, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
QuVa Pharma, Inc.
Inspection Date
March 14, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Aqualia L. Nelson (FDA Associated Person)
  • Margaret M. Annes (FDA Associated Person)
View Company Profile

ID · e60e1f85-431b-4b4b-bb92-fb5e02991b0f

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1083122
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of QuVa Pharma, Inc.

6
DateClassificationOfficeProject area
June 16, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 20, 2018Not classifiedDallas District OfficeDrug Quality Assurance
December 8, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 23, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 20, 2014OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for QuVa Pharma, Inc.
  • FDA Inspection 1172047 - 2022-06-16
  • FDA Inspection 1049888 - 2018-04-20
  • FDA Inspection 995263 - 2016-12-08
  • FDA Inspection 912138 - 2015-01-23
  • FDA Inspection 885230 - 2014-06-20

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