FDA Inspection
Pharbest Pharmaceuticals, Inc.Pharbest Pharmaceuticals, Inc. – FDA Inspection, Mar 30, 2010
Record Details
This FDA Inspection record concerns Pharbest Pharmaceuticals, Inc., with an inspection on March 30, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- March 30, 2010
- Product Type
- Drugs
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ID · 76ddc17e-92b2-49e5-a9aa-c780c70004f3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 654888
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
9- 21 CFR 211.166(b)Accelerated stability studies
- 21 CFR 211.188Prepared for each batch, include complete information
- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.180(e)Records reviewed annually
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
- 21 CFR 211.170(b)Annual visual exams of drug products
- 21 CFR 211.160(b)(4)Instruments, apparatus, et. al. not meeting specs
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Other FDA inspections of Pharbest Pharmaceuticals, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| September 15, 2025 | VAI | New York District Office | Drug Quality Assurance |
| November 10, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 3, 2021 | VAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| April 18, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 8, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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