# FDA Inspection 1078363 - Quipment Inc - February 06, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/quipment-inc/2d648546-b092-4d1a-8e08-dbb0c5e36711
Source feed: FDA_Inspections

> FDA Inspection 1078363 for Quipment Inc on February 06, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078363
- Company Name: Quipment Inc
- Inspection Date: 2019-02-06
- 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 1078363 - 2019-02-06](https://www.globalkeysolutions.net/records/fda_inspections/quipment-inc/489b1709-3f96-4ccb-93a2-b76d66be3df4)

Company: https://www.globalkeysolutions.net/companies/quipment-inc/2c9a982d-2645-44ff-8296-0f07f1235795

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