# Quipment Inc – FDA Inspection, Feb 6, 2019

Source: https://www.keypedia.com/records/fda_inspections/quipment-inc/489b1709-3f96-4ccb-93a2-b76d66be3df4
Source feed: FDA_Inspections

> FDA inspection 1078363 of Quipment Inc, February 06, 2019. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sayeeda-hdabe/eaadc7cf-5f22-47c2-ba02-437efe0a5267)

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

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