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FDA Inspection
•Intercos America, Inc.•October 9, 2024

Intercos America, Inc. – FDA Inspection, Oct 9, 2024

Record Details

This FDA Inspection record concerns Intercos America, Inc., with an inspection on October 9, 2024, issued by the New York District Office, covering human drugs.

Company
Intercos America, Inc.
Inspection Date
October 9, 2024
Product Type
Human Drugs
Office
New York District Office
People
  • Emmanuel T. Donyina (Issuing Officer)
  • Syeda N. Mahazabin (FDA Associated Person)
View Company Profile

ID · 3e29e360-e155-4544-9e7f-2465a8f797a9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1251393
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. 21 CFR 211.68(b)Computer control of master formula records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Intercos America, Inc.

5
DateClassificationOfficeProject area
June 20, 2023NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
November 24, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 28, 2011NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
May 4, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 16, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Intercos America, Inc.
  • FDA Inspection 1209614 - 2023-06-20
  • FDA Inspection 949580 - 2015-11-24
  • FDA Inspection 761254 - 2011-12-28
  • FDA Inspection 723418 - 2011-05-04
  • FDA Inspection 652199 - 2010-03-16

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