# FDA Inspection 633390 - Triplefin LLC - November 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/triplefin-llc/b14897af-44bf-4159-a1e7-11610b2fcb95
Source feed: FDA_Inspections

> FDA Inspection 633390 for Triplefin LLC on November 24, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 633390
- Company Name: Triplefin LLC
- Inspection Date: 2009-11-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 834033 - 2013-05-29](https://www.keypedia.com/records/fda_inspections/triplefin-llc/ce320472-4214-472b-8602-ef69c070d49b)
- [FDA Inspection 685150 - 2010-10-05](https://www.keypedia.com/records/fda_inspections/triplefin-llc/4e7f336c-89d8-4d57-97f2-189528ccfac3)
- [FDA Inspection 678496 - 2010-08-20](https://www.keypedia.com/records/fda_inspections/triplefin-llc/671b4de5-2ec0-46d1-8db7-00b6c9e42dff)

Company: https://www.keypedia.com/companies/triplefin-llc/132f4bc4-51fa-44ed-8813-b14a07901c78

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