# FDA Inspection 860979 - PureTek Corporation - December 18, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/puretek-corporation/a8442159-0b2b-4cf1-ae07-ab0234cddc91/
Source feed: FDA_Inspections

> FDA Inspection 860979 for PureTek Corporation on December 18, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860979
- Company Name: PureTek Corporation
- Inspection Date: 2013-12-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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

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