# FDA Inspection 1328392 - Pure Source LLC - July 28, 2026

Source: https://www.keypedia.com/records/fda_inspections/pure-source-llc/f344fe96-1822-4eb4-86df-93230ba397f5
Source feed: FDA_Inspections

> FDA Inspection 1328392 for Pure Source LLC on July 28, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1328392
- Company Name: Pure Source LLC
- Inspection Date: 2026-07-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Office Name: Florida District Office

## Related Documents

- [FDA Inspection 1328392 - 2026-07-28](https://www.keypedia.com/records/fda_inspections/pure-source-llc/814cb657-e578-4276-a0b5-88558543863c)
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- [FDA Inspection 1216969 - 2023-08-31](https://www.keypedia.com/records/fda_inspections/pure-source-llc/0cc3e2b4-5e4c-43d8-95c2-5c16ffddd3c4)
- [FDA Inspection 1099548 - 2019-08-14](https://www.keypedia.com/records/fda_inspections/pure-source-llc/1e36d227-3df3-478a-9b17-84307bb6fcae)

Company: https://www.keypedia.com/companies/pure-source-llc/442e7b43-8076-466c-8e41-0c5624502b15

Office: https://www.keypedia.com/offices/florida-district-office/95b2a118-0b78-46e0-a54c-982bd7ce51c9
