# FDA 483 - VIRGIN SCENT INC - March 11, 2022

Source: https://www.keypedia.com/records/483/virgin-scent-inc/db89389a-e516-4716-9bb3-8a1065e418e7

> FDA 483 for VIRGIN SCENT INC on March 11, 2022. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: VIRGIN SCENT INC
- Inspection Date: 2022-03-11
- Product Type: drugs
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: An FDA inspection of VIRGIN SCENT INC, an OTC drug repacker and distributor in Gardena, CA, revealed significant deficiencies in their quality system, distribution controls, and production records. The firm lacked a quality control unit, failed to maintain distribution records for hand sanitizer products, and did not prepare batch production records for repacked drugs. These findings indicate a severe lack of adherence to current Good Manufacturing Practices.

## Related Officers

- [Joel D. Hustedt](https://www.keypedia.com/people/joel-d-hustedt/29440042-08dd-4dce-be48-b55f8e1d7080)
- [issuing_officer](https://www.keypedia.com/people/gavin-t-cua/6f498dd6-2c4b-42e9-8ddc-3c2a7c97afef)

Company: https://www.keypedia.com/companies/virgin-scent-inc/62b03c7f-2f9e-45f1-b2d1-4826a2861fb0

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