# FDA Inspection 1017878 - Technicuff Corp. - July 13, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/technicuff-corp/a4b6cf67-e8d4-47c3-ac51-f49ae803a622
Source feed: FDA_Inspections

> FDA Inspection 1017878 for Technicuff Corp. on July 13, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017878
- Company Name: Technicuff Corp.
- Inspection Date: 2017-07-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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