# FDA 483 - Philips de Costa Rica S.R.L. - May 05, 2022

Source: https://www.keypedia.com/records/483/philips-de-costa-rica-srl/5bce0955-3c62-411f-94ef-299fbe6a412e

> FDA 483 for Philips de Costa Rica S.R.L. on May 05, 2022. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Philips de Costa Rica S.R.L.
- Inspection Date: 2022-05-05
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
- Summary: An FDA inspection of Philips de Costa Rica S.R.L., a medical device manufacturer in Alajuela, Costa Rica, revealed a significant deficiency in their quality system. The firm failed to adequately establish and implement procedures for corrective and preventive actions (CAPA). Specifically, their Process FMEA records did not properly define the 'Effect of Failure' as required by their own risk management procedures, indicating a breakdown in their risk assessment and CAPA processes.

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/philips-de-costa-rica-srl/1252012e-ff6f-419d-be2c-2bbc2b895b7b

Office: https://www.keypedia.com/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd