SIGVARIS DO BRASIL IND. E COM. LTDA [Jundiaí / Brazil]
SIGVARIS DO BRASIL IND. E COM. LTDA [Jundiaí / Brazil] located in JUNDIAÍ SÃO PAULO, Brazil had its last known inspection on 07 Mar 2024. There are 4 known inspections on record.
Site Details
Industries:
Medical Devices
Tags:
Medical Device Manufacturer,
Medical Devices
Last Inspection Date:
07 Mar 2024
FEI:
3004903147
Redica ID:
Investigators:
SIGVARIS DO BRASIL IND. E COM. LTDA [Jundiaí / Brazil]'s Most Recent Documents
| Publish Date | Document Type | Title |
|---|---|---|
| September, 2012 | FDA 483 | SIGVARIS DO BRASIL IND. E COM. LTDA - Form 483, 2012-09-06 |
Experience Redica Systems’ NEW site dashboards and profiles
Redica Systems customers can leverage the full Quality and Regulatory Intelligence suite, with powerful analysis covering thousands of sites around the world. You can search by FEI, or more powerfully, by the Redica ID, our universal identifier for global life sciences manufacturing sites, an industry first.
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
Loading...
Site Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to our extensive inventory of site profiles, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more