# FDA Inspection 1100229 - Precision Systems, Inc. - August 14, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/precision-systems-inc/f73b2106-d6bd-440f-90a3-6e5518294ce1/
Source feed: FDA_Inspections

> FDA Inspection 1100229 for Precision Systems, Inc. on August 14, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1100229
- Company Name: Precision Systems, Inc.
- Inspection Date: 2019-08-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100229 - 2019-08-14](https://www.globalkeysolutions.net/api/records/fda_inspections/precision-systems-inc/638df0ac-a309-4a0a-bee5-9e7fe3d952aa/)
- [FDA Inspection 833531 - 2013-05-23](https://www.globalkeysolutions.net/api/records/fda_inspections/precision-systems-inc/a0ebae0d-6611-4570-bdaa-7514f412b2a6/)
- [FDA Inspection 725010 - 2011-05-05](https://www.globalkeysolutions.net/api/records/fda_inspections/precision-systems-inc/451c422f-7699-4b3a-9ece-4698c38adff9/)

Company: https://www.globalkeysolutions.net/companies/precision-systems-inc/17098986-63c1-4dea-8b23-582f64604214

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