# Kenlor Industries, Inc. – FDA Inspection, May 3, 2019

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

> FDA inspection 1088389 of Kenlor Industries, Inc., May 03, 2019. Classification: Official Action Indicated (OAI). 10 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## 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 1021555 - 2017-06-02](https://www.keypedia.com/records/fda_inspections/kenlor-industries-inc/b41d7926-b05a-4ece-ba00-3e5371962646)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

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

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