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FDA Inspection
•Armas Eddie, MD•May 2, 2017

Armas Eddie, MD – FDA Inspection, May 2, 2017

Record Details

This FDA Inspection record concerns Armas Eddie, MD, with an inspection on May 2, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Armas Eddie, MD
Inspection Date
May 2, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Richard A. Lyght (Issuing Officer)
View Company Profile

ID · 8d568b46-fc60-4504-a299-fdbbf0f9f035

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1010183
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 Armas Eddie, MD

2
DateClassificationOfficeProject area
August 23, 2019NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
July 24, 2014NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Armas Eddie, MD
  • FDA Inspection 1101144 - 2019-08-23
  • FDA Inspection 894106 - 2014-07-24

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