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FDA Inspection
•Thibiant International, Inc.•March 15, 2018

Thibiant International, Inc. – FDA Inspection, Mar 15, 2018

Record Details

This FDA Inspection record concerns Thibiant International, Inc., with an inspection on March 15, 2018, issued by the Los Angeles District Office, covering human drugs.

Company
Thibiant International, Inc.
Inspection Date
March 15, 2018
Product Type
Human Drugs
Office
Los Angeles District Office
Person
  • Jeffrey P. Raimondi (Investigator)
View Company Profile

ID · 0d00bc22-ad30-468b-bea0-07b5c6d4073e

Inspection Facts

Inspection number
1044966
FDA center
Human Drugs
Project area
Unapproved and Misbranded Drugs
Outcome
Form 483 issued

FDA Citations

5
  1. 21 CFR 211.137(a)Expiration date lacking
  2. 21 CFR 211.166(a)Lack of written stability program
  3. 21 CFR 211.192No written record of investigation
  4. 21 CFR 211.22(d)Procedures not in writing, fully followed
  5. 21 CFR 211.84(d)(2)Reports of Analysis (Components)

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Thibiant International, Inc.

3
DateClassificationOfficeProject area
August 19, 2014VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
September 26, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 25, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Thibiant International, Inc.
  • FDA Inspection 891800 - 2014-08-19
  • FDA Inspection 850661 - 2013-09-26
  • FDA Inspection 592220 - 2009-06-25

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