# FDA Inspection 662714 - Technicuff Corp. - May 19, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/technicuff-corp/7c4a1791-48c5-47d4-a9d3-8aee95367a74
Source feed: FDA_Inspections

> FDA Inspection 662714 for Technicuff Corp. on May 19, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 662714
- Company Name: Technicuff Corp.
- Inspection Date: 2010-05-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1236757 - 2024-04-24](https://www.globalkeysolutions.net/records/fda_inspections/technicuff-corp/a11680b4-1a0e-49f3-ae6a-834516dd3f2c)
- [FDA Inspection 1236757 - 2024-04-24](https://www.globalkeysolutions.net/records/fda_inspections/technicuff-corp/f68db9dc-f3ef-4a8c-913b-ffe6305def2c)
- [FDA Inspection 1017878 - 2017-07-13](https://www.globalkeysolutions.net/records/fda_inspections/technicuff-corp/9323d3cd-c0c8-4177-ae95-2d460702bef4)
- [FDA Inspection 1017878 - 2017-07-13](https://www.globalkeysolutions.net/records/fda_inspections/technicuff-corp/a4b6cf67-e8d4-47c3-ac51-f49ae803a622)
- [FDA Inspection 883525 - 2014-06-17](https://www.globalkeysolutions.net/records/fda_inspections/technicuff-corp/8a3b4734-27cd-470d-953e-5fdbe640801d)

Company: https://www.globalkeysolutions.net/companies/technicuff-corp/c942089a-b176-4f8b-bbed-cc58b57d065d

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