# FDA Inspection 941215 - Acu Med Inc - September 08, 2015

Source: https://www.keypedia.com/records/fda_inspections/acu-med-inc/2224f987-ab40-429f-a9a8-edbfaa5a0e60
Source feed: FDA_Inspections

> FDA Inspection 941215 for Acu Med Inc on September 08, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 941215
- Company Name: Acu Med Inc
- Inspection Date: 2015-09-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 771891 - 2012-03-07](https://www.keypedia.com/records/fda_inspections/acu-med-inc/a6f6f57b-975b-4c17-be23-4c168c3f1b77)
- [FDA Inspection 608340 - 2009-04-08](https://www.keypedia.com/records/fda_inspections/acu-med-inc/321769a3-6b1b-43b5-8b7b-9bb9e51a6d92)
- [FDA Inspection 565026 - 2009-02-19](https://www.keypedia.com/records/fda_inspections/acu-med-inc/63f85286-6dab-4893-90ce-719adf6d763c)

Company: https://www.keypedia.com/companies/acu-med-inc/d4e35a0d-95c3-468e-8696-c158b56b0144

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