FDA Warning Letter — Sharplight Technologies

Case 411909 — FEI 3009352034

The FDA took a Warning Letter action against Sharplight Technologies on Nov 25, 2013 (Rishon Le-Tsiyon, Israel). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action details

Facility
Sharplight Technologies
Date
Nov 25, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Rishon Le-Tsiyon (Israel)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.