Apellis Pharmaceuticals, Inc.

FDA Regulatory Profile

Apellis Pharmaceuticals, Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2653-2023, Class II) was initiated on August 22, 2023.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2653-2023Class IIApellis Injection Kit 29g Injection Needle -single use intended to inject fluids into, or withdraw fAugust 22, 2023