FDA Inspection 1064322 - Osteotec Limited - September 04, 2018

View on Dashboard

Discuss this record with AI

ChatGPT

Claude

Perplexity

Grok

Record Details

This FDA Inspection record concerns Osteotec Limited, with an inspection on September 4, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Osteotec Limited
Inspection Date: September 4, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · c417c1aa-1fd3-4e35-9aec-db4c40769545

Violation Codes7

21 CFR 803.1721 CFR 820.198(a)21 CFR 820.2221 CFR 820.30(c)21 CFR 820.30(f)21 CFR 820.30(g)21 CFR 820.50

Full citation text and observation details available on the Dashboard.