# FDA 483 - Stryker Corporation - November 21, 2019

Source: https://www.globalkeysolutions.net/records/483/stryker-corporation/abf6d93e-220c-466e-b1d7-f683b0026ec5

> FDA 483 for Stryker Corporation on November 21, 2019. Product: device. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Stryker Corporation
- Inspection Date: 2019-11-21
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - West V
- Summary: Stryker Corporation, a medical device manufacturer in San Jose, CA, was inspected by the FDA from November 12-21, 2019. The inspection identified one observation related to the firm's complaint handling procedures. Specifically, the firm failed to establish adequate timeliness deadlines for complaint processing, resulting in several complaints not being processed in a timely manner.

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

Company: https://www.globalkeysolutions.net/companies/stryker-corporation/5d1b3e70-5dcc-4966-b0ea-0c4a31acbf43

Office: https://www.globalkeysolutions.net/offices/division-of-human-and-animal-food-operations-west-v/0f4dd01e-8e8a-4336-9abe-ce8b3d309e8b