# FDA Inspection 1088389 - Kenlor Industries, Inc. - May 03, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kenlor-industries-inc/7ed9bca3-5a78-4308-815a-4dac99abc0e7
Source feed: FDA_Inspections

> FDA Inspection 1088389 for Kenlor Industries, Inc. on May 03, 2019. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088389
- Company Name: Kenlor Industries, Inc.
- Inspection Date: 2019-05-03
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1129642 - 2020-09-21](https://www.globalkeysolutions.net/records/fda_inspections/kenlor-industries-inc/e5b441b1-d244-4e7b-af4c-4e02d45cb47b)
- [FDA Inspection 1088389 - 2019-05-03](https://www.globalkeysolutions.net/records/fda_inspections/kenlor-industries-inc/bdd02afe-d4c3-4394-a215-bb6231930f66)

Company: https://www.globalkeysolutions.net/companies/kenlor-industries-inc/cd8019cb-691d-4735-9728-add884b0aead

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