FDA Inspection
CBI Laboratories, Inc. dba Voyant Beauty LLC.CBI Laboratories, Inc. dba Voyant Beauty LLC. – FDA Inspection, May 1, 2009
Record Details
This FDA Inspection record concerns CBI Laboratories, Inc. dba Voyant Beauty LLC., with an inspection on May 1, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- May 1, 2009
- Product Type
- Drugs
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ID · 493cd6ed-f50d-4b8f-aaea-cc271ec98400
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 584934
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
8- 21 CFR 211.166(b)Adequate number of batches on stability
- 21 CFR 211.188(b)(12)Investigations made into any unexplained discrepancy
- 21 CFR 211.84(d)(2)Testing Each Component for Conformity with Specs
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
- 21 CFR 211.166(a)Results not used for expiration dates, storage cond.
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.192No written record of investigation
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Other FDA inspections of CBI Laboratories, Inc. dba Voyant Beauty LLC.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 8, 2021 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 14, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 5, 2017 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 14, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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