# FDA 483 - Vee Pak LLC - December 11, 2023

Source: https://www.keypedia.com/records/483/vee-pak-llc/16c2fa6c-2ecc-4e51-a994-afa08003d47a

> FDA 483 for Vee Pak LLC on December 11, 2023. Product: drugs. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Vee Pak LLC
- Inspection Date: 2023-12-11
- Product Type: drugs
- Office Name: Chicago District Office
- Summary: During an FDA inspection from December 6-11, 2023, Vee Pak LLC, a human drug manufacturer in Countryside, IL, was cited for deficiencies in its written stability program. The firm failed to provide adequate stability data to demonstrate the microbiological properties of several drug products remain acceptable throughout their labeled expiry period, indicating a significant quality control issue.

## Related Officers

- [Peng Zhou](https://www.keypedia.com/people/peng-zhou/ce413ab5-8787-4012-bc8f-9ef55f2c3dc1)

Company: https://www.keypedia.com/companies/vee-pak-llc/fe72be8a-7cc1-46e4-a2e0-48c8c9fb06eb

Office: https://www.keypedia.com/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669