# FDA Inspection 826422 - Dinkler Surgical Devices Inc - April 02, 2013

Source: https://www.keypedia.com/records/fda_inspections/dinkler-surgical-devices-inc/222e8f4b-d11e-4ba4-ab09-daf5363fb5ce
Source feed: FDA_Inspections

> FDA Inspection 826422 for Dinkler Surgical Devices Inc on April 02, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 826422
- Company Name: Dinkler Surgical Devices Inc
- Inspection Date: 2013-04-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 826422 - 2013-04-02](https://www.keypedia.com/records/fda_inspections/dinkler-surgical-devices-inc/c5ae34bd-94b8-44eb-9bff-2560ba17a223)
- [FDA Inspection 629984 - 2009-11-17](https://www.keypedia.com/records/fda_inspections/dinkler-surgical-devices-inc/f5d23695-ffac-433c-b8d4-c1b46125c608)

Company: https://www.keypedia.com/companies/dinkler-surgical-devices-inc/357c06e1-01ab-41c5-b8b8-7872337795b3

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