# FDA 483 - Mettler Electronics Corp - September 14, 2023

Source: https://www.keypedia.com/records/483/mettler-electronics-corp/f8daf4d6-5fd3-425b-9175-50e3ca24ce5c

> FDA 483 for Mettler Electronics Corp on September 14, 2023. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Mettler Electronics Corp
- Inspection Date: 2023-09-14
- Product Type: device
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: An FDA inspection of Mettler Electronics Corp in Anaheim, CA, revealed significant deficiencies in their quality system. The firm failed to adequately establish records for acceptable suppliers, ensure proper re-evaluation of critical suppliers, and document labeling changes for their medical devices. Additionally, personnel training for critical document change procedures was not documented, indicating a need for improved procedural adherence and record-keeping.

## Related Officers

- [Marlo-Ian M. Alintanahin](https://www.keypedia.com/people/marlo-ian-m-alintanahin/a37da927-b369-4753-b275-41743556f25e)

Company: https://www.keypedia.com/companies/mettler-electronics-corp/121e3a28-fdac-4dcc-b349-1133c5867637

Office: https://www.keypedia.com/offices/division-of-pharmaceutical-quality-operations-iv/a2d2ff91-dc0f-433e-b91f-ca90ff8998b6