# Winchester Laboratories, LLC – FDA Inspection, Jun 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/winchester-laboratories-llc/b4856889-3d83-43a3-97f3-55cc0264acf7
Source feed: FDA_Inspections

> FDA inspection 1014220 of Winchester Laboratories, LLC, June 13, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014220
- Company Name: Winchester Laboratories, LLC
- Inspection Date: 2017-06-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 774373 - 2012-03-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

Company: https://www.keypedia.com/companies/winchester-laboratories-llc/27080acb-b665-4425-806f-d68d317a1f2f

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7