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FDA Inspection
•Dario D. Altamirano, DO•September 21, 2018

Dario D. Altamirano, DO – FDA Inspection, Sep 21, 2018

Record Details

This FDA Inspection record concerns Dario D. Altamirano, DO, with an inspection on September 21, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Dario D. Altamirano, DO
Inspection Date
September 21, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Angelica M. Chica (Issuing Officer)
View Company Profile

ID · 49ae984b-e792-4681-af3d-2e79ffefe8df

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1066302
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 Dario D. Altamirano, DO

4
DateClassificationOfficeProject area
August 21, 2025Not classifiedFlorida District Office
February 9, 2022VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
June 28, 2013NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
November 3, 2011VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Dario D. Altamirano, DO
  • FDA Inspection 1279838 - 2025-08-21
  • FDA Inspection 1161913 - 2022-02-09
  • FDA Inspection 838564 - 2013-06-28
  • FDA Inspection 754975 - 2011-11-03

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