Henogen — FDA Facility Profile

FEI 3005932318

Henogen is an FDA-registered facility (FEI 3005932318) located in Seneffe, BE. Registered operations: ANALYSIS; API MANUFACTURE; LABEL; MANUFACTURE; PACK. RegDataLab tracks 1 FDA inspection at this facility.

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Facility Details

Location
Seneffe (BE)
Registration Expires
Dec 31, 2027
Operations
ANALYSIS; API MANUFACTURE; LABEL; MANUFACTURE; PACK
Source
decrs

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