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FDA Inspection
•CBI Laboratories, Inc. dba Voyant Beauty LLC.•February 14, 2014

CBI Laboratories, Inc. dba Voyant Beauty LLC. – FDA Inspection, Feb 14, 2014

Record Details

This FDA Inspection record concerns CBI Laboratories, Inc. dba Voyant Beauty LLC., with an inspection on February 14, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
CBI Laboratories, Inc. dba Voyant Beauty LLC.
Inspection Date
February 14, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 220cf0f2-2c48-41fc-a058-9381057154f4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
862837
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

6
  1. 21 CFR 211.166(b)Adequate number of batches on stability
  2. 21 CFR 211.192Quality control unit review of records
  3. 21 CFR 211.125(a)Strict control not exercised over labeling issued
  4. 21 CFR 211.100(a)Absence of Written Procedures
  5. 21 CFR 211.192Investigations of discrepancies, failures
  6. 21 CFR 211.166(a)Written program not followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of CBI Laboratories, Inc. dba Voyant Beauty LLC.

4
DateClassificationOfficeProject area
July 8, 2021OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 14, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 5, 2017OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 1, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for CBI Laboratories, Inc. dba Voyant Beauty LLC.
  • FDA Inspection 1145678 - 2021-07-08
  • FDA Inspection 1089889 - 2019-05-14
  • FDA Inspection 1033859 - 2017-12-05
  • FDA Inspection 584934 - 2009-05-01

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