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FDA Inspection
•Thornton Industries, Inc.•March 4, 2020

Thornton Industries, Inc. – FDA Inspection, Mar 4, 2020

Record Details

This FDA Inspection record concerns Thornton Industries, Inc., with an inspection on March 4, 2020, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Thornton Industries, Inc.
Inspection Date
March 4, 2020
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · d37efc18-5238-4cc7-aadb-c291ca7a8d87

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1119776
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

4
  1. 21 CFR 211.122(d)Label storage access limited to authorized personnel
  2. 21 CFR 211.165(c)Sampling and testing plans not described
  3. 21 CFR 211.84(d)(2)Component identification test
  4. 21 CFR 211.110(a)(3)Mixing adequacy

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Thornton Industries, Inc.

3
DateClassificationOfficeProject area
November 5, 2014NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
April 19, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 18, 2009NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
Other documents for Thornton Industries, Inc.
  • FDA Inspection 901828 - 2014-11-05
  • FDA Inspection 778751 - 2012-04-19
  • FDA Inspection 637094 - 2009-12-18

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