# Gresco Products, Inc. – FDA Inspection, Apr 7, 2015

Source: https://www.keypedia.com/records/fda_inspections/gresco-products-inc/3f5a1f87-0e90-4ec0-a8e0-cba79bf59e36
Source feed: FDA_Inspections

> FDA inspection 921450 of Gresco Products, Inc., April 07, 2015. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 921450
- Company Name: Gresco Products, Inc.
- Inspection Date: 2015-04-07
- 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: 10

## Related Documents

- [FDA Inspection 801268 - 2012-10-10](https://www.keypedia.com/records/fda_inspections/gresco-products-inc/36b5faa9-3182-4d5c-aa68-0e61c8b138dd)
- [FDA Inspection 726084 - 2011-06-20](https://www.keypedia.com/records/fda_inspections/gresco-products-inc/f2b23c13-eb09-4fef-9154-83cbacdf6c9e)

Company: https://www.keypedia.com/companies/gresco-products-inc/e7ded28d-7b71-4731-9947-b180a61b39b9

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