# FDA Inspection 778135 - Ernesto Rivera, MD - March 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/ernesto-rivera-md/c1bb51e0-7e84-4ee1-8a17-8a0a04cb2905
Source feed: FDA_Inspections

> FDA Inspection 778135 for Ernesto Rivera, MD on March 23, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 778135
- Company Name: Ernesto Rivera, MD
- Inspection Date: 2012-03-23
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 777071 - 2012-03-23](https://www.keypedia.com/records/fda_inspections/ernesto-rivera-md/d67cea62-4efa-4911-b04d-b7f59ba10d39)

Company: https://www.keypedia.com/companies/ernesto-rivera-md/aa48f79b-0262-4945-a1b0-6754e054ec05

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