# FDA Inspection 960739 - Pintler Medical LLC - February 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/pintler-medical-llc/d34aa306-db51-4f16-b2a2-1345cee4db80
Source feed: FDA_Inspections

> FDA Inspection 960739 for Pintler Medical LLC on February 23, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960739
- Company Name: Pintler Medical LLC
- Inspection Date: 2016-02-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 960739 - 2016-02-23](https://www.keypedia.com/records/fda_inspections/pintler-medical-llc/f168da48-637c-4634-9784-dede194efc79)
- [FDA Inspection 857575 - 2013-11-21](https://www.keypedia.com/records/fda_inspections/pintler-medical-llc/7a92f4a4-a90f-447a-bd9c-da7fedd96846)
- [FDA Inspection 857575 - 2013-11-21](https://www.keypedia.com/records/fda_inspections/pintler-medical-llc/30c0084c-76e3-4578-b77e-743e679ab0e3)

Company: https://www.keypedia.com/companies/pintler-medical-llc/9d680fe5-dd0b-4009-9873-2e744c061b74

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