FDA Inspection
Hammill Manufacturing CompanyHammill Manufacturing Company – FDA Inspection, Nov 17, 2017
Record Details
This FDA Inspection record concerns Hammill Manufacturing Company, with an inspection on November 17, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Amy S. Graf (Issuing Officer)
View Company Profile
ID · 43602571-2b1f-4e92-a3b2-086cf17ed553
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1031576
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
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Other FDA inspections of Hammill Manufacturing Company
5| Date | Classification | Office | Project area |
|---|---|---|---|
| March 13, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 30, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 24, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 2, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 10, 2008 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Hammill Manufacturing Company
- FDA Inspection 1264299 - 2025-03-13
- FDA Inspection 911740 - 2015-01-30
- FDA Inspection 800297 - 2012-09-24
- FDA Inspection 610841 - 2009-09-02
- FDA Inspection 538700 - 2008-11-10
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