# Kenlor Industries, Inc. – FDA Inspection, Jun 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/kenlor-industries-inc/b41d7926-b05a-4ece-ba00-3e5371962646
Source feed: FDA_Inspections

> FDA inspection 1021555 of Kenlor Industries, Inc., June 02, 2017. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021555
- Company Name: Kenlor Industries, Inc.
- Inspection Date: 2017-06-02
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Los Angeles District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1129642 - 2020-09-21](https://www.keypedia.com/records/fda_inspections/kenlor-industries-inc/e5b441b1-d244-4e7b-af4c-4e02d45cb47b)
- [FDA Inspection 1088389 - 2019-05-03](https://www.keypedia.com/records/fda_inspections/kenlor-industries-inc/7ed9bca3-5a78-4308-815a-4dac99abc0e7)

## Related Officers

- Issuing Officer

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

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b