# FDA Inspection 803728 - Rite-dent Manufacturing Corp. - August 28, 2012

Source: https://www.keypedia.com/records/fda_inspections/rite-dent-manufacturing-corp/0b8795e4-f91d-4c5d-9e37-fd2e3dffbd6e
Source feed: FDA_Inspections

> FDA Inspection 803728 for Rite-dent Manufacturing Corp. on August 28, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803728
- Company Name: Rite-dent Manufacturing Corp.
- Inspection Date: 2012-08-28
- 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 803728 - 2012-08-28](https://www.keypedia.com/records/fda_inspections/rite-dent-manufacturing-corp/362c9777-03f4-447f-8add-955d61ab0caa)
- [FDA Inspection 698163 - 2010-11-16](https://www.keypedia.com/records/fda_inspections/rite-dent-manufacturing-corp/50d53fea-6b38-454f-9135-083475ab9606)
- [FDA Inspection 698163 - 2010-11-16](https://www.keypedia.com/records/fda_inspections/rite-dent-manufacturing-corp/53ef3489-8f03-4259-b522-b1465dc2a726)
- [FDA Inspection 670603 - 2010-07-08](https://www.keypedia.com/records/fda_inspections/rite-dent-manufacturing-corp/1ae0cc0b-730b-49ec-821f-ec957437589f)
- [FDA Inspection 670603 - 2010-07-08](https://www.keypedia.com/records/fda_inspections/rite-dent-manufacturing-corp/366ab175-ff89-43d3-87bb-ba1048639553)

Company: https://www.keypedia.com/companies/rite-dent-manufacturing-corp/2e538c71-21a2-4835-afdd-9e4ac6b89197

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