# FDA Inspection 939661 - Mederi Therapeutics, Inc - August 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/mederi-therapeutics-inc/8597ea20-e1cc-4074-9d48-fd604bd02751
Source feed: FDA_Inspections

> FDA Inspection 939661 for Mederi Therapeutics, Inc on August 19, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939661
- Company Name: Mederi Therapeutics, Inc
- Inspection Date: 2015-08-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 939661 - 2015-08-19](https://www.keypedia.com/records/fda_inspections/mederi-therapeutics-inc/68d93a44-0858-49a8-b8ac-213a7d53cc38)
- [FDA Inspection 796568 - 2012-08-29](https://www.keypedia.com/records/fda_inspections/mederi-therapeutics-inc/63518bea-d556-478f-a57e-fb051b65af84)
- [FDA Inspection 632101 - 2009-12-03](https://www.keypedia.com/records/fda_inspections/mederi-therapeutics-inc/604409ff-1f53-4adf-a925-a9619e03a347)

Company: https://www.keypedia.com/companies/mederi-therapeutics-inc/d3011a90-1d63-4196-ac54-27f4d8b26156

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