21 C.F.R. § 820.150 Storage.
Title 21 - Food and Drugs
(a) Each manufacturer shall establish and maintain procedures for the control of storage areas and stock rooms for product to prevent mixups, damage, deterioration, contamination, or other adverse effects pending use or distribution and to ensure that no obsolete, rejected, or deteriorated product is used or distributed. When the quality of product deteriorates over time, it shall be stored in a manner to facilitate proper stock rotation, and its condition shall be assessed as appropriate. (b) Each manufacturer shall establish and maintain procedures that describe the methods for authorizing receipt from and dispatch to storage areas and stock rooms.
Title 21: Food and Drugs
PART 820—QUALITY SYSTEM REGULATION
Subpart L—Handling, Storage, Distribution, and Installation
§ 820.150 Storage.
