FDA Inspection
Neutraderm Inc.Neutraderm Inc. – FDA Inspection, Jul 2, 2009
Record Details
This FDA Inspection record concerns Neutraderm Inc., with an inspection on July 2, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Neutraderm Inc.
- Inspection Date
- July 2, 2009
- Product Type
- Drugs
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ID · 0a06ecc2-22e3-44e4-8a64-4ca81e77851e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 595797
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.63Equipment Design, Size and Location
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
- 21 CFR 211.100(a)Absence of Written Procedures
- 21 CFR 211.67(b)Written procedures not established/followed
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Other FDA inspections of Neutraderm Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2026 | Not classified | Los Angeles District Office | |
| December 9, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 14, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 22, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 26, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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