# FDA Inspection 1195354 - Springboard Manufacturing - January 12, 2023

Source: https://www.keypedia.com/records/fda_inspections/springboard-manufacturing/c8452518-d780-48c2-9418-34edf9f1feb1
Source feed: FDA_Inspections

> FDA Inspection 1195354 for Springboard Manufacturing on January 12, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195354
- Company Name: Springboard Manufacturing
- Inspection Date: 2023-01-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195354 - 2023-01-12](https://www.keypedia.com/records/fda_inspections/springboard-manufacturing/cd1adc46-6873-4097-8767-27eaca89c654)

Company: https://www.keypedia.com/companies/springboard-manufacturing/a80e1326-05a3-4a9e-8ee4-260257767a6e

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