# Coopervision Manufacturing, Ltd – FDA Inspection, Jan 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/coopervision-manufacturing-ltd/74b2a6e8-c5ca-4dc2-bb03-ef124d9bf9b5
Source feed: FDA_Inspections

> FDA inspection 1076150 of Coopervision Manufacturing, Ltd, January 10, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1076150
- Company Name: Coopervision Manufacturing, Ltd
- Inspection Date: 2019-01-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- FDA Inspection 1079354 - 2019-01-17
- FDA Inspection 1006523 - 2017-01-19
- [FDA Inspection 859895 - 2013-12-05](https://www.keypedia.com/records/fda_inspections/coopervision-manufacturing-ltd/b598e19a-86ae-4684-bf96-96ab3631ef90)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/coopervision-manufacturing-ltd/364600de-7712-44eb-a131-78eaf65112eb

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8