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FDA Inspection
•Trinity Enterprise Inc•February 18, 2011

Trinity Enterprise Inc – FDA Inspection, Feb 18, 2011

Record Details

This FDA Inspection record concerns Trinity Enterprise Inc, with an inspection on February 18, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Trinity Enterprise Inc
Inspection Date
February 18, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · b0a8ba34-e3f2-4e32-861d-8f52f2853c85

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
711749
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

3
  1. 21 CFR 820.198(c)Investigation of device failures
  2. 21 CFR 820.198(e)Records of complaint investigation
  3. 21 CFR 820.50(b)Supplier notification of changes

Full citation text and observation details available on the Dashboard.

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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