FDA Inspection
Dermarite Industries, LLC.Dermarite Industries, LLC. – FDA Inspection, Mar 3, 2011
Record Details
This FDA Inspection record concerns Dermarite Industries, LLC., with an inspection on March 3, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Dermarite Industries, LLC.
- Inspection Date
- March 3, 2011
- Product Type
- Drugs
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ID · 7d2ade7a-15f8-4129-9ffa-1fe3da0d3447
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 710120
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.103Actual vs. theoretical yields not determined
- 21 CFR 211.166(b)Adequate number of batches on stability
- 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
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Other FDA inspections of Dermarite Industries, LLC.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 8, 2025 | Not classified | New Jersey District Office | |
| April 8, 2025 | OAI | New Jersey District Office | Drug Quality Assurance |
| October 10, 2018 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 30, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 23, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Dermarite Industries, LLC.
- FDA Inspection 1276408 - 2025-07-08
- FDA Inspection 1250450 - 2025-04-08
- FDA Inspection 1068298 - 2018-10-10
- FDA Inspection 1030174 - 2017-10-30
- FDA Inspection 915250 - 2015-02-23
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