# FDA 483 - Moebius Precision Corporation - September 26, 2025

Source: https://www.keypedia.com/records/483/moebius-precision-corporation/77cda62f-e9bc-4637-8c0a-f0913d42b393

> FDA 483 for Moebius Precision Corporation on September 26, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Moebius Precision Corporation
- Inspection Date: 2025-09-26
- Product Type: device
- Office Name: Detroit District Office
- Summary: An FDA inspection of Moebius Precision Corporation, a medical device manufacturer in Lansing, MI, revealed significant deficiencies across its quality system. The firm failed to adequately establish procedures for corrective and preventive actions, control of nonconforming products, training, and document control. These issues indicate a lack of robust quality management practices within the facility.

## Related Officers

- [David J. Gasparovich](https://www.keypedia.com/people/david-j-gasparovich/478888db-d4b3-481a-89f5-ee234a160f07)

Company: https://www.keypedia.com/companies/moebius-precision-corporation/5e06cf4f-2eaa-45f6-aa97-2e07ce03a2d5

Office: https://www.keypedia.com/offices/detroit-district-office/b09a1815-a000-40c0-bb44-5432ce87ed03