# Cramer Products Inc – FDA Inspection, Oct 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/cramer-products-inc/f23e735e-732f-4fe4-9b0c-e489d362e156
Source feed: FDA_Inspections

> FDA inspection 946520 of Cramer Products Inc, October 26, 2015. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 946520
- Company Name: Cramer Products Inc
- Inspection Date: 2015-10-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1009621 - 2017-04-14](https://www.keypedia.com/records/fda_inspections/cramer-products-inc/3b99d158-cd06-4788-a845-0793ae774fd5)
- FDA Inspection 755637 - 2011-12-05
- [FDA Inspection 645205 - 2010-01-20](https://www.keypedia.com/records/fda_inspections/cramer-products-inc/c9510d67-c1bf-497e-8406-a18cf3942ca3)

Company: https://www.keypedia.com/companies/cramer-products-inc/d7e7fa6d-0836-47a2-9d5f-a59def20b4e7

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