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FDA Inspection
•Todd Bertoch, M.D.•September 27, 2024

Todd Bertoch, M.D. – FDA Inspection, Sep 27, 2024

Record Details

This FDA Inspection record concerns Todd Bertoch, M.D., with an inspection on September 27, 2024, issued by the Denver District Office, covering human drugs.

Company
Todd Bertoch, M.D.
Inspection Date
September 27, 2024
Product Type
Human Drugs
Office
Denver District Office
Person
  • Logan M. Jones (Investigator)
View Company Profile

ID · ff8a5e49-30e9-463a-9db4-a29273f7ae69

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1250219
FDA center
Human Drugs
Project area
Bioresearch Monitoring: Human Drugs
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 312.60FD-1572, protocol compliance

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Todd Bertoch, M.D.

2
DateClassificationOfficeProject area
January 9, 2026NAIBioresearch Monitoring
December 12, 2022NAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
Other documents for Todd Bertoch, M.D.
  • FDA Inspection 1301790 - 2026-01-09
  • FDA Inspection 1194405 - 2022-12-12

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