# FDA 483 - Pulsar Scientific LLC - May 06, 2026

Source: https://www.keypedia.com/records/483/pulsar-scientific-llc/a1675065-090b-40a1-befe-90c001157ea0

> FDA 483 for Pulsar Scientific LLC on May 06, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Pulsar Scientific LLC
- Inspection Date: 2026-05-06
- Product Type: device
- Office Name: New England District Office
- Summary: An FDA inspection of Pulsar Scientific LLC, a medical device manufacturer in Ludlow, MA, identified one significant observation. The firm failed to submit required Unique Device Identifier (UDI) information to the FDA's Global Unique Device Identification Database (GUDID) for its Recovery+ thermal compression system prior to commercial distribution. This indicates a lapse in regulatory compliance regarding device identification.

## Related Officers

- [Eric C. Schmitt](https://www.keypedia.com/people/eric-c-schmitt/f2716c8c-f06e-4519-a1e7-63a3ef6e07fb)

Company: https://www.keypedia.com/companies/pulsar-scientific-llc/71ede31c-01b4-4453-adcf-c06732ce7def

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144