FDA Inspection
New Jersey LaboratoriesNew Jersey Laboratories – FDA Inspection, Sep 23, 2016
Record Details
This FDA Inspection record concerns New Jersey Laboratories, with an inspection on September 23, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- New Jersey Laboratories
- Inspection Date
- September 23, 2016
- Product Type
- Drugs
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ID · ac64564d-a7a9-4372-9e46-6f2356856688
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 987775
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.160(a)Following/documenting laboratory controls
- 21 CFR 211.160(b)(4)Establishment of calibration procedures
- 21 CFR 211.165(e)Test methods
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of New Jersey Laboratories
6| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2026 | Not classified | New Jersey District Office | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| September 22, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 12, 2017 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| July 9, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 29, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for New Jersey Laboratories
- FDA Inspection 1318216 - 2026-05-12
- FDA Inspection 1180024 - 2022-09-22
- FDA Inspection 1009479 - 2017-04-12
- FDA Inspection 887267 - 2014-07-09
- FDA Inspection 787570 - 2012-06-29
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