# HLPR, Inc. dba Lakewood Products – FDA Inspection, Dec 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/hlpr-inc-dba-lakewood-products/03e149c6-d543-45bf-b596-5d12f68bbee8
Source feed: FDA_Inspections

> FDA inspection 1034598 of HLPR, Inc. dba Lakewood Products, December 05, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034598
- Company Name: HLPR, Inc. dba Lakewood Products
- Inspection Date: 2017-12-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/benjamin-w-anderson/a3c0961c-6a83-4bd7-abb8-02c5c8dd3a35)

Company: https://www.keypedia.com/companies/hlpr-inc-dba-lakewood-products/f1d0583a-523b-43d2-988f-81b4f278225f

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