# PureTek Corporation – FDA Inspection, Jul 16, 2010

Source: https://www.keypedia.com/records/fda_inspections/puretek-corporation/b9cffb91-8b6c-4880-860e-ed3928a7ca80
Source feed: FDA_Inspections

> FDA inspection 675510 of PureTek Corporation, July 16, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 211. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675510
- Company Name: PureTek Corporation
- Inspection Date: 2010-07-16
- 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: 3

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Company: https://www.keypedia.com/companies/puretek-corporation/428846ad-3d0d-4e9e-9b5e-41321940234c

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