FDA Inspection
Westwood Laboratories, LLC.Westwood Laboratories, LLC. – FDA Inspection, Aug 2, 2019
Record Details
This FDA Inspection record concerns Westwood Laboratories, LLC., with an inspection on August 2, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c1e68d81-591b-4321-838c-24c58c3f2985
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1098876
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.184DHR content
- 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
- 21 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Westwood Laboratories, LLC.
12| Date | Classification | Office | Project area |
|---|---|---|---|
| March 26, 2026 | Not classified | Los Angeles District Office | Drug Quality Assurance |
| October 31, 2024 | OAI | Los Angeles District Office | Drug Quality Assurance |
| November 20, 2023 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 5, 2022 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| May 30, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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