# FDA 483 - Blickman Industries LLC - August 20, 2021

Source: https://www.keypedia.com/records/483/blickman-industries-llc/2384a1cf-55a0-47e5-a426-dcff857911e7

> FDA 483 for Blickman Industries LLC on August 20, 2021. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Blickman Industries LLC
- Inspection Date: 2021-08-20
- Product Type: device
- Office Name: New Jersey District Office
- Summary: Blickman Industries LLC, a manufacturer and distributor of medical metal stands, carts, tables, and cabinetry in Clifton, NJ, received a Form 483 citing significant deficiencies in its quality system. The inspection revealed a lack of established procedures for Unique Device Identification (UDI) and inadequate supplier management, including insufficient documentation of supplier agreements and audits. Additionally, the firm failed to submit a Medical Device Report (MDR) for a serious injury and exhibited poor document control with unauthorized personnel approving critical revisions.

## Related Documents

- [483 - 2025-03-21](https://www.keypedia.com/records/483/blickman-industries-llc/95e992c6-b188-4e68-9a30-a2eebd8550f3)

## Related Officers

- [Michelle L Johnson](https://www.keypedia.com/people/michelle-l-johnson/7a31a805-4066-41ec-9f65-f1f907695044)
- [David H. Smith](https://www.keypedia.com/people/david-h-smith/a78c3b20-1fb4-438f-904b-a6ab51a81945)

Company: https://www.keypedia.com/companies/blickman-industries-llc/44c486cd-a566-4c36-bde6-fd08e3446983

Office: https://www.keypedia.com/offices/new-jersey-district-office/6ff5e2e9-5cff-44c7-af24-5a55329a8248