# FDA Inspection 826676 - HTL - March 07, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/htl/ce8439ff-6010-4b43-be17-0c5493c8e643
Source feed: FDA_Inspections

> FDA Inspection 826676 for HTL on March 07, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 826676
- Company Name: HTL
- Inspection Date: 2013-03-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/htl/87ec999b-4336-4ba0-903d-7a63728978c3

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