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FDA Inspection
•Joseph F. Fowler, Jr., M.D.•August 16, 2017

Joseph F. Fowler, Jr., M.D. – FDA Inspection, Aug 16, 2017

Record Details

This FDA Inspection record concerns Joseph F. Fowler, Jr., M.D., with an inspection on August 16, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Joseph F. Fowler, Jr., M.D.
Inspection Date
August 16, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Karen M. Cooper (Company Rep)
View Company Profile

ID · 397b6132-ff43-4138-9339-5a0ff87bcb5a

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1021764
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 312.60FD-1572, protocol compliance
  2. 21 CFR 312.66Unanticipated problems
  3. 21 CFR 312.62(a)Accountability records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Joseph F. Fowler, Jr., M.D.

1
DateClassificationOfficeProject area
July 28, 2011NAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
Other documents for Joseph F. Fowler, Jr., M.D.
  • FDA Inspection 737387 - 2011-07-28

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