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FDA Inspection
•Jeanelle L. Kam, M.D.•June 7, 2019

Jeanelle L. Kam, M.D. – FDA Inspection, Jun 7, 2019

Record Details

This FDA Inspection record concerns Jeanelle L. Kam, M.D., with an inspection on June 7, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Jeanelle L. Kam, M.D.
Inspection Date
June 7, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Andrace Deyampert (FDA Associated Person)
  • Travis M. Beard (Company Rep)
View Company Profile

ID · 9bbd8043-e770-4238-a8c6-6eda0932bae5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1095770
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 312.57(c)Record retention requirement

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Jeanelle L. Kam, M.D.

2
DateClassificationOfficeProject area
November 18, 2022VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
February 28, 2017Not classifiedDallas District Office
Other documents for Jeanelle L. Kam, M.D.
  • FDA Inspection 1192116 - 2022-11-18
  • FDA Inspection 1004057 - 2017-02-28

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