# FDA 483 - Westridge Laboratories Inc - January 18, 2023

Source: https://www.globalkeysolutions.net/records/483/westridge-laboratories-inc/f3c96e6f-9f26-455d-82d2-e581e953ce40

> FDA 483 for Westridge Laboratories Inc on January 18, 2023. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Westridge Laboratories Inc
- Inspection Date: 2023-01-18
- Product Type: drugs
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: Westridge Laboratories Inc, a manufacturer in Santa Ana, CA, was cited for deficiencies in its complaint handling procedures. The firm failed to include required justifications for not conducting investigations for certain complaints, even when an adverse reaction was reported. This indicates a lapse in maintaining complete and compliant complaint records.

## Related Documents

- [483 - 2025-12-29](https://www.globalkeysolutions.net/records/483/westridge-laboratories-inc/1dcce1f9-cd4a-4215-8fe6-83eae992b55a)

## Related Officers

- [Kevin N. Tran](https://www.globalkeysolutions.net/people/kevin-n-tran/dd74120c-4a8d-4fd0-9068-c862890d00d6)

Company: https://www.globalkeysolutions.net/companies/westridge-laboratories-inc/342e0eb1-1bc3-4619-9d4a-842a82f4c536

Office: https://www.globalkeysolutions.net/offices/division-of-pharmaceutical-quality-operations-iv/a2d2ff91-dc0f-433e-b91f-ca90ff8998b6