# FDA 483 - Natureplex LLC - July 24, 2025

Source: https://www.globalkeysolutions.net/records/483/natureplex-llc/814cc5c9-ef39-4342-961b-b28da96f4076

> FDA 483 for Natureplex LLC on July 24, 2025. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Natureplex LLC
- Inspection Date: 2025-07-24
- Product Type: drugs
- Office Name: New Orleans District Office
- Summary: Natureplex LLC, a drug manufacturer in Olive Branch, MS, received a Form 483 citing significant deficiencies in its quality control unit and investigation procedures. The inspection revealed inadequate laboratory investigations, unaddressed consumer complaints, and insufficient stability studies, indicating a failure to ensure drug products meet cGMP standards for safety, efficacy, purity, and quality. These issues highlight a systemic lack of oversight and thoroughness in quality management processes.

## Related Documents

- [483 - 2019-12-20](https://www.globalkeysolutions.net/records/483/natureplex-llc/b0cb31ca-d151-47f1-a586-a6e5f3b94b79)

## Related Officers

- [Medical Officer at FDA](https://www.globalkeysolutions.net/people/brittny-c-cargo/a3479241-5390-4ddb-b892-df0bac1c89cf)

Company: https://www.globalkeysolutions.net/companies/natureplex-llc/05ad1dc9-b4af-4dfc-970f-5a91aaf229ce

Office: https://www.globalkeysolutions.net/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea