FAQ-Suzhou Pharma Cleanroom Validation in Saudi Arabia
2022-04-20
Our Suzhou Pharma Cleanroom passed SFDA Test in Saudi Arabia, and it was already in production the products in early of 2022.
How can make it easier for our customers to pass the FDA test?
1. The hepa filter and hepa box has inspection report&certificate .(IEST-CC034-001)
2. All cleanroom materials has CE certificate documents. And windows with CCC certificate.
3. Some electric parts with UL certificate as request.
If you will build an cleanroom for GMP standard production area, please contact Suzhou Pharma design and do turnkey solution for you.
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Telephone: +86-18241958031/
+86-18913598640
Fax: 86-512-65488640
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