# Hammill Manufacturing Company – FDA Inspection, Nov 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/hammill-manufacturing-company/43602571-2b1f-4e92-a3b2-086cf17ed553
Source feed: FDA_Inspections

> FDA inspection 1031576 of Hammill Manufacturing Company, November 17, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031576
- Company Name: Hammill Manufacturing Company
- Inspection Date: 2017-11-17
- 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: 2

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- FDA Inspection 911740 - 2015-01-30
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- [FDA Inspection 538700 - 2008-11-10](https://www.keypedia.com/records/fda_inspections/hammill-manufacturing-company/68eaa94d-fb2b-4f49-b4b5-74ec1dd8bf8f)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/hammill-manufacturing-company/4e443170-6ab3-41a7-b26c-8d4ef9ab1f8a

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