# FDA 483 - Active Life Scientific, Inc - June 11, 2025

Source: https://www.globalkeysolutions.net/records/483/active-life-scientific-inc/09468c18-b2e9-401b-9aff-73dea5bfc129

> FDA 483 for Active Life Scientific, Inc on June 11, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Active Life Scientific, Inc
- Inspection Date: 2025-06-11
- Product Type: device
- Office Name: Los Angeles District Office
- Summary: An FDA inspection of Active Life Scientific, Inc. in Santa Barbara, CA, a medical device manufacturer, identified one observation related to inadequate procedures for device history records. Specifically, the firm's DHRs for the OsteoProbe System did not clearly indicate the final manufacturing date or include the device label and identifier. This indicates a moderate severity issue concerning quality system documentation for medical devices.

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

Company: https://www.globalkeysolutions.net/companies/active-life-scientific-inc/1911540b-ce9d-4d94-ba04-c56cb9d5e5d7

Office: https://www.globalkeysolutions.net/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b