# FDA Inspection 1226525 - Precipart Corp - December 20, 2023

Source: https://www.keypedia.com/records/fda_inspections/precipart-corp/841faba5-207c-4657-81c1-a640f34edbb2
Source feed: FDA_Inspections

> FDA Inspection 1226525 for Precipart Corp on December 20, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1226525
- Company Name: Precipart Corp
- Inspection Date: 2023-12-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1226525 - 2023-12-20](https://www.keypedia.com/records/fda_inspections/precipart-corp/8b207fdd-0900-47c2-935b-cbb128a9915b)
- [FDA Inspection 1136295 - 2021-02-25](https://www.keypedia.com/records/fda_inspections/precipart-corp/271f508b-91c8-4800-98e7-113fde08cc73)
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- [FDA Inspection 1041079 - 2018-02-09](https://www.keypedia.com/records/fda_inspections/precipart-corp/51d86fc3-f467-4ee4-acb4-20f8ad94d3e8)

Company: https://www.keypedia.com/companies/precipart-corp/23370f3c-d19d-4cd2-9369-c9c780b57c5a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7