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FDA Inspection
•Andrew C Sedillo, MD•September 3, 2026

Andrew C Sedillo, MD – FDA Inspection, Sep 3, 2026

Record Details

This FDA Inspection record concerns Andrew C Sedillo, MD, with an inspection on September 3, 2026, issued by the Denver District Office, covering human drugs.

Company
Andrew C Sedillo, MD
Inspection Date
September 3, 2026
Product Type
Human Drugs
Office
Denver District Office
Person
  • Gavin W. Pierce (Issuing Officer)
View Company Profile

ID · 55683424-1fab-433c-bffe-18964e40e053

Inspection Facts

Inspection number
1334832
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

1
  1. 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 Andrew C Sedillo, MD

4
DateClassificationOfficeProject area
May 7, 2025VAIDenver District OfficeBioresearch Monitoring: Human Drugs
October 11, 2019NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
February 16, 2018NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
June 2, 2016VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Andrew C Sedillo, MD
  • FDA Inspection 1269750 - 2025-05-07
  • FDA Inspection 1108035 - 2019-10-11
  • FDA Inspection 1044979 - 2018-02-16
  • FDA Inspection 982272 - 2016-06-02

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