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FDA Inspection
•Kay Chemical Company•December 5, 2025

Kay Chemical Company – FDA Inspection, Dec 5, 2025

Record Details

This FDA Inspection record concerns Kay Chemical Company, with an inspection on December 5, 2025, issued by the Atlanta District Office, covering human drugs.

Company
Kay Chemical Company
Inspection Date
December 5, 2025
Product Type
Human Drugs
Office
Atlanta District Office
Person
  • Tammy T. Brown (Company Rep)
View Company Profile

ID · cf90f4cf-cb91-4a42-a2fc-40624243b8ea

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1294076
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 211.113(a)Procedures for non-sterile drug products
  2. 21 CFR 211.166(a)(2)Stability sample storage conditions described

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Kay Chemical Company

3
DateClassificationOfficeProject area
October 8, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 30, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 12, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Kay Chemical Company
  • FDA Inspection 1110551 - 2019-10-08
  • FDA Inspection 912805 - 2015-01-30
  • FDA Inspection 720753 - 2011-04-12

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