# FDA Inspection 1148524 - Litex Manufacturing, Inc - August 05, 2021

Source: https://www.globalkeysolutions.net/records/fda_inspections/litex-manufacturing-inc/f7f94bac-991e-4b8a-8a07-1cddde1c6074/
Source feed: FDA_Inspections

> FDA Inspection 1148524 for Litex Manufacturing, Inc on August 05, 2021. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1148524
- Company Name: Litex Manufacturing, Inc
- Inspection Date: 2021-08-05
- 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 1148524 - 2021-08-05](https://www.globalkeysolutions.net/api/records/fda_inspections/litex-manufacturing-inc/52ff68de-b0dc-4270-a232-d6ed89159cf4/)
- [FDA Inspection 1064722 - 2018-08-13](https://www.globalkeysolutions.net/api/records/fda_inspections/litex-manufacturing-inc/13a03b49-ea27-4a47-a8b0-fa514410640a/)
- [FDA Inspection 1064722 - 2018-08-13](https://www.globalkeysolutions.net/api/records/fda_inspections/litex-manufacturing-inc/7c53ec54-51d1-40d5-b888-5ad1b7fce38e/)

Company: https://www.globalkeysolutions.net/companies/litex-manufacturing-inc/6e7e4274-e9c4-49f9-a01a-c9e9e8a2fc98

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