# FDA Inspection 982340 - Implant Direct Sybron International, LLC - June 28, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/implant-direct-sybron-international-llc/6a61471f-26c4-4cc9-8387-89e56babdbac
Source feed: FDA_Inspections

> FDA Inspection 982340 for Implant Direct Sybron International, LLC on June 28, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982340
- Company Name: Implant Direct Sybron International, LLC
- Inspection Date: 2016-06-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 988719 - 2016-08-29](https://www.globalkeysolutions.net/records/fda_inspections/implant-direct-sybron-international-llc/eb18bade-1e60-46b3-a5fa-daf5a2103e14)
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Company: https://www.globalkeysolutions.net/companies/implant-direct-sybron-international-llc/484fcb7c-406d-4a2e-9056-486a8496908b

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