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FDA Inspection
•Lynn R. Webster, MD•March 24, 2017

Lynn R. Webster, MD – FDA Inspection, Mar 24, 2017

Record Details

This FDA Inspection record concerns Lynn R. Webster, MD, with an inspection on March 24, 2017, issued by the Denver District Office, covering human drugs.

Company
Lynn R. Webster, MD
Inspection Date
March 24, 2017
Product Type
Human Drugs
Office
Denver District Office
Person
  • Stephen T. Hansen (Company Rep)
View Company Profile

ID · 84b483b9-7294-4d4e-a2fa-8c4f7c2fbee3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1007143
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 312.60FD-1572, protocol compliance
  2. 21 CFR 312.62(b)Case history records- inadequate or inadequate

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Lynn R. Webster, MD

5
DateClassificationOfficeProject area
July 21, 2015NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
July 10, 2015NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
August 22, 2013VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
December 2, 2011NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
January 18, 2010NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Lynn R. Webster, MD
  • FDA Inspection 935057 - 2015-07-21
  • FDA Inspection 932176 - 2015-07-10
  • FDA Inspection 846633 - 2013-08-22
  • FDA Inspection 756109 - 2011-12-02
  • FDA Inspection 638829 - 2010-01-18

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