# FDA Inspection 962626 - Rehrig Pacific Company - March 03, 2016

Source: https://www.keypedia.com/records/fda_inspections/rehrig-pacific-company/f2f810f8-40f3-4ace-9fcc-ae94d71a0783
Source feed: FDA_Inspections

> FDA Inspection 962626 for Rehrig Pacific Company on March 03, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 962626
- Company Name: Rehrig Pacific Company
- Inspection Date: 2016-03-03
- 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 962626 - 2016-03-03](https://www.keypedia.com/records/fda_inspections/rehrig-pacific-company/900aeee7-0de6-40c3-aed8-eed1ca0b1117)

Company: https://www.keypedia.com/companies/rehrig-pacific-company/0d6a7faa-f50e-4ba3-ac96-cda0965fdd93

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