# FDA 483 - Vitalant - May 09, 2019

Source: https://www.keypedia.com/records/483/vitalant/60470075-30e3-4384-889f-31d109a7b706

> FDA 483 for Vitalant on May 09, 2019. Product: biologics. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Vitalant
- Inspection Date: 2019-05-09
- Product Type: biologics
- Office Name: New Orleans District Office
- Summary: Vitalant in Memphis, TN, was inspected from May 6-9, 2019, and received a Form 483. The inspection revealed deficiencies related to the proper observation, standardization, and calibration of equipment used in blood and blood component collection. Specifically, a component collection machine was found to be in use without proper leveling, and the firm's SOP lacked instructions for this critical step.

## Related Officers

- [Christopher J. Adams](https://www.keypedia.com/people/christopher-j-adams/f7010846-7fd1-4ee8-901a-1015656fea0a)

Company: https://www.keypedia.com/companies/vitalant/6c2a2531-72ae-4697-ab09-75caffe15162

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