# Ultradent Products, Inc. – FDA Inspection, Sep 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/ultradent-products-inc/f53c1f50-8e3a-4190-9346-3baafd7f0a1e
Source feed: FDA_Inspections

> FDA inspection 1025250 of Ultradent Products, Inc., September 15, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 211. Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025250
- Company Name: Ultradent Products, Inc.
- Inspection Date: 2017-09-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 1

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/haroon-vohra/690c60b4-3059-4768-bfca-0cdabc58a72a)

Company: https://www.keypedia.com/companies/ultradent-products-inc/16b4d8af-54bd-48d3-acc8-a5169bd5bfe3

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c