FDA Inspection
Almark Tool & Manufacturing Company, Inc.Almark Tool & Manufacturing Company, Inc. – FDA Inspection, May 20, 2013
Record Details
This FDA Inspection record concerns Almark Tool & Manufacturing Company, Inc., with an inspection on May 20, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- May 20, 2013
- Product Type
- Devices
View Company Profile
ID · 292a7f0d-1a7b-43c3-a3af-0def33f06bec
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 832436
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Almark Tool & Manufacturing Company, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 7, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 24, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 15, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Almark Tool & Manufacturing Company, Inc.
- FDA Inspection 1196549 - 2023-02-07
- FDA Inspection 1041346 - 2018-01-24
- FDA Inspection 907128 - 2014-12-15
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