FDA Inspection
Dermarite Industries, LLC.Dermarite Industries, LLC. – FDA Inspection, Feb 23, 2015
Record Details
This FDA Inspection record concerns Dermarite Industries, LLC., with an inspection on February 23, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Dermarite Industries, LLC.
- Inspection Date
- February 23, 2015
- Product Type
- Drugs
View Company Profile
ID · e6dafd43-83ee-4089-b707-3187bcdeb579
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 915250
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.63Equipment Design, Size and Location
- 21 CFR 211.84(d)(1)Identity Testing of Each Component
Full citation text and observation details available on the Dashboard.
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 |
| May 10, 2012 | 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 780318 - 2012-05-10
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.