# FDA Inspection 1081601 - Dentamerica - February 12, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/dentamerica/d8e5d952-c0b8-45db-93a6-f14abd1c42dd
Source feed: FDA_Inspections

> FDA Inspection 1081601 for Dentamerica on February 12, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1081601
- Company Name: Dentamerica
- Inspection Date: 2019-02-12
- 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 1081601 - 2019-02-12](https://www.globalkeysolutions.net/records/fda_inspections/dentamerica/b2f392f6-7862-40c6-8e2c-6ecee9610f5e)
- [FDA Inspection 893140 - 2014-08-25](https://www.globalkeysolutions.net/records/fda_inspections/dentamerica/c89d25aa-b1e5-4f81-b7f2-e3668cc764a6)
- [FDA Inspection 893140 - 2014-08-25](https://www.globalkeysolutions.net/records/fda_inspections/dentamerica/348b05dc-c5c6-42c5-b074-b9ff25034e16)
- [FDA Inspection 761078 - 2011-12-20](https://www.globalkeysolutions.net/records/fda_inspections/dentamerica/959cf0ba-23c9-422c-bd75-253896b0cbf4)

Company: https://www.globalkeysolutions.net/companies/dentamerica/d35485f3-976c-4199-8f39-0c325261141d

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