# Ultralite Enterprises Inc – FDA Inspection, Jan 29, 2009

Source: https://www.keypedia.com/records/fda_inspections/ultralite-enterprises-inc/7b914b34-0f24-4a66-9528-68105ce00c6d
Source feed: FDA_Inspections

> FDA inspection 570532 of Ultralite Enterprises Inc, January 29, 2009. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 570532
- Company Name: Ultralite Enterprises Inc
- Inspection Date: 2009-01-29
- 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: 1

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Company: https://www.keypedia.com/companies/ultralite-enterprises-inc/38d8b2bf-c1f4-4e43-bfdd-6f1ea477254b

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