# Almark Tool & Manufacturing Company, Inc. – FDA Inspection, May 20, 2013

Source: https://www.keypedia.com/records/fda_inspections/almark-tool-manufacturing-company-inc/292a7f0d-1a7b-43c3-a3af-0def33f06bec
Source feed: FDA_Inspections

> FDA inspection 832436 of Almark Tool & Manufacturing Company, Inc., May 20, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 832436
- Company Name: Almark Tool & Manufacturing Company, Inc.
- Inspection Date: 2013-05-20
- 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

## Related Documents

- [FDA Inspection 1196549 - 2023-02-07](https://www.keypedia.com/records/fda_inspections/almark-tool-manufacturing-company-inc/89851e88-73bb-4ef0-b180-39604bb07a6f)
- FDA Inspection 1041346 - 2018-01-24
- FDA Inspection 907128 - 2014-12-15

Company: https://www.keypedia.com/companies/almark-tool-manufacturing-company-inc/2bb5c682-e451-4888-b310-fe8babaf9e85

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