# FDA Inspection 837704 - Hu-Friedy Mfg Co, Inc. - July 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/hu-friedy-mfg-co-inc/4d67b9a5-b89e-4da0-bc92-47f59aaad643
Source feed: FDA_Inspections

> FDA Inspection 837704 for Hu-Friedy Mfg Co, Inc. on July 10, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 837704
- Company Name: Hu-Friedy Mfg Co, Inc.
- Inspection Date: 2013-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 837704 - 2013-07-10](https://www.keypedia.com/records/fda_inspections/hu-friedy-mfg-co-inc/0218717f-4e06-4317-863a-cf7aa83dc4c9)
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Company: https://www.keypedia.com/companies/hu-friedy-mfg-co-inc/60d31633-54f1-42c3-b732-e86a80535f85

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