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FDA Inspection
•Thibiant International, Inc.•September 26, 2013

Thibiant International, Inc. – FDA Inspection, Sep 26, 2013

Record Details

This FDA Inspection record concerns Thibiant International, Inc., with an inspection on September 26, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Thibiant International, Inc.
Inspection Date
September 26, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · bb639a30-d9cd-475c-82f7-728434ad0d15

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
850661
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.22(b)Adequate lab facilities not available
  2. 21 CFR 211.137(a)Expiration date lacking
  3. 21 CFR 211.192No written record of investigation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Thibiant International, Inc.

3
DateClassificationOfficeProject area
March 15, 2018Not classifiedLos Angeles District OfficeUnapproved and Misbranded Drugs
August 19, 2014VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
June 25, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Thibiant International, Inc.
  • FDA Inspection 1044966 - 2018-03-15
  • FDA Inspection 891800 - 2014-08-19
  • FDA Inspection 592220 - 2009-06-25

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