# FDA Inspection 985219 - Lonza Bend Inc. - June 03, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/lonza-bend-inc/2d358c56-966e-4c56-b316-5e35ed462134
Source feed: FDA_Inspections

> FDA Inspection 985219 for Lonza Bend Inc. on June 03, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985219
- Company Name: Lonza Bend Inc.
- Inspection Date: 2016-06-03
- 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/lonza-bend-inc/35de45c5-ab00-4ab8-a472-a01f6edc8897

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